4,4,4-Trifluorobutanoic acid → HCID 178520631, compound

HRID 1909368Notes

Reaction equation

HRID 1909368 reaction equation
Cl.[O:2]1[C:6]2[CH:7]=[CH:8][CH:9]=[C:10]([CH:11]3[CH2:16][CH2:15][N:14]([CH2:17][CH2:18][C@H:19]4[CH2:24][CH2:23][C@H:22]([NH2:25])[CH2:21][CH2:20]4)[CH2:13][CH2:12]3)[C:5]=2[O:4][CH2:3]1.[F:26][C:27]([F:34])([F:33])[CH2:28][CH2:29][C:30](O)=[O:31]>>[O:2]1[C:6]2[CH:7]=[CH:8][CH:9]=[C:10]([CH:11]3[CH2:16][CH2:15][N:14]([CH2:17][CH2:18][C@H:19]4[CH2:20][CH2:21][C@H:22]([NH:25][C:30](=[O:31])[CH2:29][CH2:28][C:27]([F:34])([F:33])[F:26])[CH2:23][CH2:24]4)[CH2:13][CH2:12]3)[C:5]=2[O:4][CH2:3]1

Participants

3

Reactant 2

HCID 27770854,4,4-Trifluorobutanoic acidHCID 178479251HCID 178479251, compound2×

Product 1

HCID 178520631HCID 178520631, compound

Procedure

The title compound, white solid (12.8 mg, 35.2%), MS (ISP) m/z=455.4 [(M+H)+], was prepared in accordance with the general method of example 1 from Trans-4-[2-(4-Benzo[1,3]dioxol-4-yl-piperidin-1-yl)-ethyl]-cyclohexylamine hydrochloride (intermediate A) (29.4 mg, 0.080 mmol) and 4,4,4-trifluorobutanoic acid

Sources & evidence

ORD record
ord-43598d72ca2a478fabb684ba23cba4d0
Source dataset
uspto-grants-2013_12
Patent number
US08598357B2

Reaction notes

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