HCID 15711979, compound → HCID 67870328, compound

Reaction equation

[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[NH:8][C:7]([CH3:13])([CH3:12])[CH:6]=[C:5]2[N:14]1[CH2:18][CH2:17][CH2:16][C:15]1=[O:19].C(C1C=C2C(=CC=1)NC(C)(C)C=C2N1CCCC1=[O:39])#N>>[CH3:13][C:7]1([CH3:12])[C@@H:6]([OH:39])[C@H:5]([N:14]2[CH2:18][CH2:17][CH2:16][C:15]2=[O:19])[C:4]2[C:9](=[CH:10][CH:11]=[C:2]([Br:1])[CH:3]=2)[NH:8]1

Participants

Reactant 2

HCID 15711979HCID 15711979, compound

HCID 15711981HCID 15711981, compound

Product 1

HCID 67870328HCID 67870328, compound

Procedure

A method according to claim 11, wherein the compound of formula (I) is 6-bromo-2,2-dimethyl-4-(2-oxo-1-pyrrolidinyl)-1,2-dihydroquinoline or 6-cyano-2,2-dimethyl-4-(2-oxo-1-pyrrolidinyl)-1,2-dihydroquinoline.

Sources & evidence

ORD record: ord-a8dac5e71a164a20a5989768898fe160
Source dataset: uspto-grants-1989_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04808619

Reaction notes

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