Methanol → N-((1-(2-(3-tert-butylureido)ethyl)piperidin-4-yl)methyl)-3,5-bis(trifluoromethyl)benzamide

HRID 508634Notes

Reaction equation

HRID 508634 reaction equation
[NH2:1][CH2:2][CH2:3][N:4]1[CH2:9][CH2:8][CH:7]([CH2:10][NH:11][C:12](=[O:27])[C:13]2[CH:18]=[C:17]([C:19]([F:22])([F:21])[F:20])[CH:16]=[C:15]([C:23]([F:26])([F:25])[F:24])[CH:14]=2)[CH2:6][CH2:5]1.[C:28]([N:32]=[C:33]=[O:34])([CH3:31])([CH3:30])[CH3:29].CO>C(Cl)Cl>[C:28]([NH:32][C:33](=[O:34])[NH:1][CH2:2][CH2:3][N:4]1[CH2:5][CH2:6][CH:7]([CH2:10][NH:11][C:12](=[O:27])[C:13]2[CH:18]=[C:17]([C:19]([F:21])([F:22])[F:20])[CH:16]=[C:15]([C:23]([F:24])([F:25])[F:26])[CH:14]=2)[CH2:8][CH2:9]1)([CH3:31])([CH3:30])[CH3:29]

Participants

5

Procedure

A solution of N-((1-(2-aminoethyl)piperidin-4-yl)methyl)-3,5-bis(trifluoromethyl)benzamide (25 mg, 0.063 mmol) in CH2Cl2 (1.5 mL) was treated with t-butyl isocyanate (30 mg, 0.13 mmol). The mixture was stirred overnight, treated with MeOH (1 mL). The solvent was removed in vacuo. The residue was purified by HiTOPs.

Workup

  1. customThe solvent was removed in vacuo
  2. customThe residue was purified by HiTOPs

Sources & evidence

ORD record
ord-bcbf395b56884623a90abc2fd5664150
Source dataset
uspto-grants-2015_08
Patent number
US09096522B2

Reaction notes

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