Trifluoroacetic acid → HCID 18613135, compound

HRID 1265824Notes

Reaction equation

HRID 1265824 reaction equation
C(OC(=O)[NH:7][C:8]1[CH:13]=[C:12]([N:14]([CH3:16])[CH3:15])[C:11]([C:17]([F:20])([F:19])[F:18])=[CH:10][C:9]=1[NH:21][C:22](=[O:46])[CH2:23][C:24](=O)[C:25]1[CH:30]=[CH:29][CH:28]=[C:27]([C:31]2[N:32]([CH2:36][CH2:37][O:38]C3CCCCO3)[N:33]=[CH:34][CH:35]=2)[CH:26]=1)(C)(C)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[CH3:16][N:14]([CH3:15])[C:12]1[C:11]([C:17]([F:20])([F:19])[F:18])=[CH:10][C:9]2[NH:21][C:22](=[O:46])[CH2:23][C:24]([C:25]3[CH:30]=[CH:29][CH:28]=[C:27]([C:31]4[N:32]([CH2:36][CH2:37][OH:38])[N:33]=[CH:34][CH:35]=4)[CH:26]=3)=[N:7][C:8]=2[CH:13]=1

Participants

4

Procedure

The title compound was prepared from (RS)-{5-dimethylamino-2-[3-oxo-3-(3-{2-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-2H-pyrazol-3-yl}-phenyl)-propionylamino]-4-trifluoromethyl-phenyl}-carbamic acid tert.-butyl ester (Example M69) (237 mg, 0.36 mmol) by treatment with TFA in CH2Cl2 according to the general procedure N. Obtained as an off-white solid (48 mg).

Sources & evidence

ORD record
ord-42567f2ecc15404cae8c7db23ca970a3
Source dataset
uspto-grants-2003_04
Patent number
US06544985B2

Reaction notes

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