1-[(5-Bromo-2-thienyl)carbonyl]pyrrolidine → {2-Fluoro-4-[5-(pyrrolidine-1-carbonyl)-thiophen-2-yl]-phenyl}-[2-(S)-(2-(R)-methyl-pyrrolidin-1-ylmethyl)-pyrrolidin-1-yl]-methanone

HRID 646442Notes

Reaction equation

HRID 646442 reaction equation
[F:1][C:2]1[CH:7]=[C:6](B2OC(C)(C)C(C)(C)O2)[CH:5]=[CH:4][C:3]=1[C:17]([N:19]1[CH2:23][CH2:22][CH2:21][C@H:20]1[CH2:24][N:25]1[CH2:29][CH2:28][CH2:27][C@H:26]1[CH3:30])=[O:18].Br[C:32]1[S:36][C:35]([C:37]([N:39]2[CH2:43][CH2:42][CH2:41][CH2:40]2)=[O:38])=[CH:34][CH:33]=1>>[F:1][C:2]1[CH:7]=[C:6]([C:32]2[S:36][C:35]([C:37]([N:39]3[CH2:43][CH2:42][CH2:41][CH2:40]3)=[O:38])=[CH:34][CH:33]=2)[CH:5]=[CH:4][C:3]=1[C:17]([N:19]1[CH2:23][CH2:22][CH2:21][C@H:20]1[CH2:24][N:25]1[CH2:29][CH2:28][CH2:27][C@H:26]1[CH3:30])=[O:18]

Participants

3

Procedure

The title compound is prepared in a manner substantially analogous to General Procedure A using [2-Fluoro-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-[2-(S)-(2-(R)-methyl-pyrrolidin-1-ylmethyl)-pyrrolidin-1-yl]-methanone (408 mg, 0.98 mmol) and (5-Bromo-thiophen-2-yl)-pyrrolidin-1-yl-methanone (CAS 326875) (256 mg) MS 470.2 (M+H)+

Sources & evidence

ORD record
ord-0024f470cdc5405f96a359406a0e28a9
Source dataset
uspto-grants-2010_04
Patent number
US07705025B2

Reaction notes

Loading…