Benzene, 1-(1-bromopropyl)-4-(trifluoromethoxy)- → 5-(2,6-Dimethoxyphenyl)-3-methyl-1-(1-(4-(trifluoromethoxy)phenyl)propyl)pyrrolidin-2-one

HRID 594621Notes

Reaction equation

HRID 594621 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([O:9][CH3:10])[C:4]=1[CH:11]1[NH:15][C:14](=[O:16])[CH:13]([CH3:17])[CH2:12]1.Br[CH:19]([C:22]1[CH:27]=[CH:26][C:25]([O:28][C:29]([F:32])([F:31])[F:30])=[CH:24][CH:23]=1)[CH2:20][CH3:21]>>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([O:9][CH3:10])[C:4]=1[CH:11]1[N:15]([CH:19]([C:22]2[CH:23]=[CH:24][C:25]([O:28][C:29]([F:30])([F:31])[F:32])=[CH:26][CH:27]=2)[CH2:20][CH3:21])[C:14](=[O:16])[CH:13]([CH3:17])[CH2:12]1

Participants

3

Procedure

Prepared according to the described general procedure 4 (GP4) by reaction of 5-(2,6-dimethoxyphenyl)-3-methylpyrrolidin-2-one with 1-(1-bromopropyl)-4-(trifluoromethoxy)-benzene. Subsequent purification by preparative HPLC afforded the target compound. LC-MS (conditions A): tR=1.00 min.; [M+H]+: 438.28 g/mol.

Workup

  1. customPrepared
  2. customSubsequent purification by preparative HPLC
  3. customafforded the target compound

Sources & evidence

ORD record
ord-3e5891a2aa3c40d1bcbb803e0f0335c8
Source dataset
uspto-grants-2016_01
Patent number
US09242970B2

Reaction notes

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