3,3,3-Trifluoropropanal → HCID 75047737, compound

HRID 1951103Notes

Reaction equation

HRID 1951103 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[CH2:12][N:11]([C:13]([CH:15]3[CH2:20][CH2:19][NH:18][CH2:17][CH2:16]3)=[O:14])[CH2:10][CH:9]2[N:21]([CH3:36])[C:22](=[O:35])[C:23]2[CH:28]=[CH:27][C:26]([O:29][CH3:30])=[C:25]([C:31]([F:34])([F:33])[F:32])[CH:24]=2)=[CH:4][CH:3]=1.[F:37][C:38]([F:43])([F:42])[CH2:39][CH:40]=O>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]2[CH2:12][N:11]([C:13]([CH:15]3[CH2:20][CH2:19][N:18]([CH2:40][CH2:39][C:38]([F:43])([F:42])[F:37])[CH2:17][CH2:16]3)=[O:14])[CH2:10][CH:9]2[N:21]([CH3:36])[C:22](=[O:35])[C:23]2[CH:28]=[CH:27][C:26]([O:29][CH3:30])=[C:25]([C:31]([F:33])([F:32])[F:34])[CH:24]=2)=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 680283,3,3-TrifluoropropanalHCID 67025677HCID 67025677, compound

Product 1

HCID 75047737HCID 75047737, compound

Procedure

In analogy to the procedure described for the synthesis of example 104, the title compound N-{(3RS,4SR)-4-(4-chloro-phenyl)-1-[1-(3,3,3-trifluoro-propyl)-piperidine-4-carbonyl]-pyrrolidin-3-yl}-4-methoxy-N-methyl-3-trifluoromethyl-benzamide was prepared from N-[(3RS,4SR)-4-(4-chloro-phenyl)-1-(piperidine-4-carbonyl)-pyrrolidin-3-yl]-4-methoxy-N-methyl-3-trifluoromethyl-benzamide using 3,3,3-trifluoropropanal instead of acetone and was obtained as a light brown oil. MS m/e: 620.3 [M]+.

Workup

  1. customIn analogy to the procedure described for the synthesis of example 104
  2. customwas obtained as a light brown oil

Sources & evidence

ORD record
ord-8810a3c33852499f8ec3f6a54874b85b
Source dataset
uspto-grants-2013_03
Patent number
US08404679B2

Reaction notes

Loading…