3,5-Bis(trifluoromethyl)benzoyl chloride → HCID 60196491, compound

HRID 878220Notes

Reaction equation

HRID 878220 reaction equation
[O:1]1[CH2:4][CH:3]([NH:5][C:6]2[CH:7]=[N:8][CH:9]=[CH:10][C:11]=2[C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[CH3:18])[CH2:2]1.[F:19][C:20]([F:35])([F:34])[C:21]1[CH:22]=[C:23]([CH:27]=[C:28]([C:30]([F:33])([F:32])[F:31])[CH:29]=1)[C:24](Cl)=[O:25]>CCCCCCC.CCOC(C)=O>[O:1]1[CH2:2][CH:3]([N:5]([C:6]2[CH:7]=[N:8][CH:9]=[CH:10][C:11]=2[C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[CH3:18])[C:24](=[O:25])[C:23]2[CH:27]=[C:28]([C:30]([F:31])([F:32])[F:33])[CH:29]=[C:21]([C:20]([F:19])([F:34])[F:35])[CH:22]=2)[CH2:4]1

Participants

4

Procedure

The title compound was prepared in analogy to example 72, intermediate, from oxetan-3-yl-(4-o-tolyl-pyridin-3-yl)-amine and 3,5-bis(trifluoromethyl)benzoyl chloride (CAS RN 1271-19-8) and using a gradient of gradient of n-heptane:EtOAc (100:0 to 30:70) for the chromatographic purification. Light yellow solid (34%). MS (ESI): m/z=481.13 [M+H]+.

Workup

  1. customfor the chromatographic purification

Sources & evidence

ORD record
ord-cf3ee7c54b0e4ebcb3c77d5df15409e3
Source dataset
uspto-grants-2015_03
Patent number
US08987307B2

Reaction notes

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