Trifluoroacetic acid → HCID 59463765, compound

HRID 1713380Notes

Reaction equation

HRID 1713380 reaction equation
C(O)(C(F)(F)F)=O.C(OC(=O)[NH:14][CH2:15][CH:16]([CH2:27][O:28][C:29]([C:42]1[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1)([C:36]1[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=1)[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)[CH2:17][CH2:18][N:19]1[CH:24]=[CH:23][C:22](=[O:25])[NH:21][C:20]1=[O:26])(C)(C)C>ClCCl>[NH2:14][CH2:15][CH:16]([CH2:27][O:28][C:29]([C:42]1[CH:43]=[CH:44][CH:45]=[CH:46][CH:47]=1)([C:36]1[CH:37]=[CH:38][CH:39]=[CH:40][CH:41]=1)[C:30]1[CH:31]=[CH:32][CH:33]=[CH:34][CH:35]=1)[CH2:17][CH2:18][N:19]1[CH:24]=[CH:23][C:22](=[O:25])[NH:21][C:20]1=[O:26]

Participants

4

Procedure

TFA (2 ml) was added to a solution of compound 42 (100 mg, 0.18 mmol) in dichloromethane (4 ml) and the solution was stirred at room temperature. After 30 min the solvents were evaporated in vacuo and the afforded residue was purified by column chromatography on silica gel which gave the title compound (52 mg, 65%).

Workup

  1. customAfter 30 min the solvents were evaporated in vacuo
  2. customthe afforded residue was purified by column chromatography on silica gel which

Sources & evidence

ORD record
ord-42437e22a4a9426ca8b5b017153d67ff
Source dataset
uspto-grants-2010_09
Patent number
US07795270B2

Reaction notes

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