US2010210495A1PendingUtilityA1
Photo-labile pro-fragrance conjugates
Est. expiryNov 8, 2020(expired)· nominal 20-yr term from priority
C07C 235/34A61Q 5/02A61K 2800/57A61K 8/0229A61Q 19/10C07D 207/38C11D 3/507A61Q 15/00A61Q 5/12A61Q 13/00C07D 265/06A61K 8/49C07D 263/04A61K 8/35
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Claims
Abstract
The present invention relates to photo-labile pro-fragrance conjugates comprising: a) a photo-labile unit which upon exposure to electromagnetic radiation is capable of releasing a pro-fragrance unit; and b) a pro-fragrance unit, which when so released is either i) a pro-fragrance compound capable of releasing a fragrance raw material; or ii) a fragrance raw material. The present invention relates to systems for delivering fragrances to a situs, and to laundry detergent compositions, fine fragrances, personal care and hair care compositions comprising said systems.
Claims
exact text as granted — not AI-modified1 . A photo-activated pro-fragrance conjugate comprising:
a) a photo-labile unit which upon exposure to electromagnetic radiation is capable of releasing a pro-fragrance unit; and b) a pro-fragrance unit comprising at least one nitrogen atom, and an optional linking moiety, said at least one nitrogen atom being bound directly to said photo-labile unit, or indirectly to said photo-labile unit by said linking moiety, via a chemical bond capable of being broken when said conjugate is exposed to electromagnetic radiation.
2 . A conjugate according to claim 1 wherein said pro-fragrance unit has the formula:
wherein each R 3 is independently selected from hydrogen, substituted or unsubstituted C 1 -C 30 hydrocarbyl, and mixtures thereof.
3 . A conjugate according to claim 1 comprising said optional linking moiety.
4 . A conjugate according to claim 2 comprising said optional linking moiety.
5 . A conjugate according to claim 1 having Formula I or II:
wherein each R 1 is independently hydrogen, a unit which can substitute for hydrogen selected from the group consisting of:
a) —NHCOR 30 ;
b) —COR 30 ;
c) —COOR 30 ;
d) —COCH═CH 2 ;
e) —C(═NH)NH 2 ;
f) —N(R 30 ) 2 ;
g) —NHC 6 H 5 ;
h) —CON(R 30 ) 2 ;
i) —CONHNH 2 ;
j) —NHCN;
k) —OCN;
l) —CN;
m) F, Cl, Br, I, and mixtures thereof;
n) —OR 30 ;
o) —NHCHO;
p) —OH;
q) —NHN(R 30 ) 2 ;
r) —NHOR 30 ;
s) —CNO;
t) —NCS;
u) —SO 3 M;
v) —OSO 3 M;
w) —SCN;
x) —P(O)H 2 ;
y) —PO 2 ;
z) —P(O)(OH) 2 ;
aa) —SO 2 NH 2 ;
ab) —SO 2 R 30 ;
ac) —NO 2;
ad) —CF 3 , —CCl 3 , —CBr 3 ;
ae) and mixtures thereof,
or a C 1 -C 12 substituted or unsubstituted hydrocarbyl unit, R 30 is hydrogen, C 1 -C 20 linear or branched alkyl, C 6 -C 20 aryl, C 7 -C 20 alkylenearyl, and mixtures thereof; M is hydrogen, or a salt forming cation;
each R 2 is independently hydrogen, a C 1 -C 12 substituted or unsubstituted hydrocarbyl unit, and mixtures thereof;
X is —OH or —NHR 12 ; and R 12 is H, C 1 -C 12 substituted or unsubstituted alkyl, and mixtures thereof.
6 . A conjugate according to claim 5 wherein said pro-fragrance unit has the formula:
wherein each R 3 is independently selected from hydrogen, substituted or unsubstituted C 1 -C 30 hydrocarbyl, and mixtures thereof.
7 . A conjugate according to claim 6 comprising said optional linking moiety.
8 . A conjugate according to claim 2 wherein said pro-fragrance unit has the formula:
wherein each R 4 is independently selected from the group consisting of:
a) hydrogen;
b) C 1 -C 22 substituted or unsubstituted, branched or unbranched alkyl;
c) C 2 -C 22 substituted or unsubstituted, branched or unbranched alkenyl;
d) C 2 -C 20 substituted or unsubstituted, branched or unbranched hydroxyalkyl;
e) C 7 -C 20 substituted or unsubstituted alkylenearyl;
f) C 3 -C 20 substituted or unsubstituted cycloalkyl;
g) C 6 -C 20 aryl;
h) C 5 -C 20 heteroaryl units comprising one or more heteroatoms selected from the group consisting of nitrogen, oxygen, sulfur, and mixtures thereof;
i) and mixtures thereof;
any two R 4 units may optionally covalently bind together, when said any two R 4 units optionally covalently bind together said any two R 4 units form a moiety selected from the group consisting of aromatic or non-aromatic, heterocyclic or non-heterocyclic, single rings, fused rings, bicyclo rings, spiroannulated rings, or mixtures thereof, said rings comprising from 3 to 20 carbon atoms and one or more heteroatoms selected from the group consisting of nitrogen, oxygen, sulfur, and mixtures thereof; and
G 1 and G 2 are each independently hydrogen, C 1 -C 20 linear or branched hydrocarbyl, —Y, —C(O)Y, and mixtures thereof; Y is C 6 -C 10 substituted or unsubstituted cyclic alkyl.
9 . A conjugate according to claim 2 wherein said pro-fragrance unit has the formula:
wherein Z is oxygen or sulfur; and the index m is 1, 2 or 3.
R 5 is a substituted or unsubstituted hydrocarbyl unit which comprises:
a) a C 6 -C 22 substituted or unsubstituted, linear or branched alkyl or alkenyl;
b) a C 6 -C 22 substituted or unsubstituted: cycloalkyl, branched cycloalkyl, cycloalkenyl, branched cycloalkenyl, aryl, heterocyclicalkyl, or heterocyclicalkenyl
c) and mixtures thereof;
R 6 comprises:
a) hydrogen;
b) a C 1 -C 10 substituted or unsubstituted linear alkyl;
c) a C 3 -C 10 substituted or unsubstituted branched alkyl;
d) a C 2 -C 10 substituted or unsubstituted linear alkenyl;
e) a C 3 -C 10 substituted or unsubstituted branched alkenyl;
f) a C 3 -C 15 substituted or unsubstituted cycloalkyl;
g) a C 4 -C 15 substituted or unsubstituted branched cycloalkyl;
h) a C 4 -C 15 substituted or unsubstituted cycloalkenyl;
i) a C 5 -C 15 substituted or unsubstituted branched cycloalkenyl;
j) a C 6 -C 15 substituted or unsubstituted aryl;
k) a C 6 -C 22 substituted or unsubstituted heterocyclicalkyl;
l) a C 6 -C 22 substituted or unsubstituted heterocyclicalkenyl;
m) and mixtures thereof;
said R 5 and R 6 units may optionally, when taken together, form a substituted or unsubstituted ring comprising a ring moiety, said ring moiety comprising from 3 to 10 carbon atoms;
each R 7 is independently a substituted or unsubstituted hydrocarbyl unit; when taken together, any two geminal R 7 units form a carbonyl moiety, or when any two R 7 units covalently bind together, said R 7 units form a moiety selected from the group consisting of:
i) a C 3 -C 6 spiroannulated ring;
ii) a heterocyclic aromatic ring comprising from 5 to 7 atoms;
iii) a non-heterocyclic aromatic ring comprising from 5 to 7 atoms;
iv) a heterocyclic ring comprising from 5 to 7 atoms;
v) a non-heterocyclic ring comprising from 5 to 7 atoms;
vi) or mixtures thereof; and
the index m is an integer from 1 to 3.
10 . A composition comprising:
a) a photo-activated pro-fragrance conjugate according to claim 1 ; and b) the balance carriers and adjunct ingredients.
11 . A photo-labile pro-fragrance conjugate delivery system comprising:
a) from about 0.001% by weight, of a photo-activated pro-fragrance conjugate according to claim 1 ; and b) the balance carriers and adjunct ingredients.
12 . A laundry detergent comprising:
a) from about 0.001% by weight, of a photo-activated pro-fragrance conjugate according to claim 1 ; b) from about 10% by weight, of a detersive surfactant; and c) the balance carriers and adjunct ingredients.
13 . Perfume or fine fragrance comprising:
a) from about 0.001% by weight, of a photo-activated pro-fragrance conjugate according to claim 1 ; b) from about 0.01% to about 99% by weight, of an admixture of fragrance raw materials; and c) the balance carriers and adjunct ingredients.
14 . A hair shampoo or conditioner comprising:
a) from about 0.001% by weight, of a photo-activated pro-fragrance conjugate according to claim 1 ; b) from about 0.01% to about 5% by weight, of an admixture of fragrance raw materials; and c) the balance carriers and adjunct ingredients.Cited by (0)
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