2-Methylpyrrolidine → HCID 71556752, compound

HRID 1497146Notes

Reaction equation

C[O:2][C:3]([C:5]1[C:6](Cl)=[N:7][C:8]2[C:13]([C:14]=1[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)=[CH:12][C:11]([CH2:21][CH3:22])=[CH:10][C:9]=2[CH3:23])=[O:4].[CH3:25][CH:26]1[CH2:30][CH2:29][CH2:28][NH:27]1>>[CH2:21]([C:11]1[CH:12]=[C:13]2[C:8](=[C:9]([CH3:23])[CH:10]=1)[N:7]=[C:6]([N:27]1[CH2:28][CH2:29][CH2:30][CH:26]1[CH3:25])[C:5]([C:3]([OH:2])=[O:4])=[C:14]2[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[CH3:22]

Participants

Reactant 2

HCID 130032-Methylpyrrolidine

HCID 86682987HCID 86682987, compound

Product 1

HCID 71556752HCID 71556752, compound

Procedure

The title compound was prepared in analogy to example 54 step F from 2-chloro-6-ethyl-8-methyl-4-phenyl-quinoline-3-carboxylic acid methyl ester (prepared as described in example 54 step E) and 2-methylpyrrolidine. Light brown solid. MS (ESI): 375.3 (M+H)+.

Sources & evidence

ORD record: ord-3436413d9cf14bc8b90f540f72b61e01
Source dataset: uspto-grants-2015_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09199938B2

Reaction notes

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