US2012302793A1PendingUtilityA1
Aromatic amine derivative and organic electroluminescent device using same
Est. expiryJan 5, 2025(expired)· nominal 20-yr term from priority
H10K 50/00C09K 11/06C07C 211/61C07C 2603/26C07C 2603/97H05B 33/14C09K 2211/1011H05B 33/20C07C 2603/50C09K 2211/1007C07C 211/58C07C 2603/18Y10S428/917C07C 211/54H10K 50/14H10K 50/11H10K 85/633H10K 85/626H10K 85/324H10K 85/649
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Claims
Abstract
A process for producing an amine compound, by reacting a halogenated aryl compound with an amine intermediate of formula (1): wherein: Ar 1 is a substituted or unsubstituted aryl group comprising 6 to 50 ring atoms; and R 1 and R 2 are each independently an alkyl group comprising 1 to 50 carbon atoms, which may together form a cyclic structure.
Claims
exact text as granted — not AI-modified1 - 20 . (canceled)
21 . A process for producing an amine compound, the process comprising:
(I) reacting a halogenated aryl compound with an amine intermediate of formula (1):
wherein:
Ar 1 is a substituted or unsubstituted aryl group comprising 6 to 50 ring atoms; and
R 1 and R 2 are each independently an alkyl group comprising 1 to 50 carbon atoms, which may together form a cyclic structure.
22 . The process of claim 21 , wherein the reacting (I) is carried out in the presence of a base and a palladium compound.
23 . The process of claim 21 , wherein the halogenated aryl compound comprises a nitrogen atom.
24 . The process of claim 21 , wherein the halogenated aryl is a compound is selected from the group consisting of compounds:
25 . The process of claim 24 , wherein the halogenated aryl compound is:
26 . The process of claim 24 , wherein the halogenated aryl compound is:
27 . The process of claim 21 , wherein the amine intermediate has a formula selected from the group consisting of formulae:
28 . The process of claim 21 , wherein the amine intermediate has formula (2):
wherein:
R 1 to R 4 are each independently an alkyl group comprising 1 to 50 carbon atoms, and provided that R 1 and R 2 may together form a cyclic structure, and R 3 and R 4 may together form a cyclic structure.
29 . The process of claim 28 , wherein the amine intermediate is:
30 . The process of claim 21 , wherein the amine intermediate has formula (3):
wherein R 1 and R 2 are each independently an alkyl group comprising 1 to 50 carbon atoms, which may together form a cyclic structure.
31 . The process of claim 30 , wherein said reacting is carried out in the presence of a base and a palladium compound.
32 . The process of claim 30 , wherein the halogenated aryl compound comprises a nitrogen atom.
33 . The process of claim 30 , wherein the halogenated aryl compound is selected from the group consisting of the compounds:
34 . The process of claim 33 , wherein the halogenated aryl compound is:
35 . The process of claim 33 , wherein the halogenated aryl compound is:
36 . The process of claim 30 , wherein the amine intermediate has a formula selected from the group consisting of formulae:
37 . The process of claim 36 , wherein the amine intermediate has a formula:
38 . The process of claim 36 , wherein the amine intermediate has a formula:
39 . The process of claim 36 , wherein the amine intermediate has a formula:Join the waitlist — get patent alerts
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