Trifluoroacetic acid → HCID 22224841, compound
Reaction equation
C(OC(=O)[NH:7][C:8]1[CH:13]=[CH:12][C:11]([C:14]#[C:15][C:16]2[CH:21]=CC(F)=[CH:18][CH:17]=2)=[CH:10][C:9]=1[NH:23][C:24](=[O:36])[CH2:25][C:26]([C:28]1[CH:33]=[CH:32][CH:31]=[C:30]([C:34]#[N:35])[CH:29]=1)=O)(C)(C)C.[C:38](O)([C:40]([F:43])(F)F)=O>C(Cl)Cl>[F:43][C:40]1[CH:38]=[CH:21][C:16]([C:15]#[C:14][C:11]2[CH:12]=[CH:13][C:8]3[N:7]=[C:26]([C:28]4[CH:29]=[C:30]([CH:31]=[CH:32][CH:33]=4)[C:34]#[N:35])[CH2:25][C:24](=[O:36])[NH:23][C:9]=3[CH:10]=2)=[CH:17][CH:18]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Prepared from [2-[3-(3-cyano-phenyl)-3-oxo-propionylamino]-4-(4-fluoro-phenylethynyl)-phenyl]-carbamic acid tert.-butyl ester (Example K98) (307 mg, 0.62 mmol) by treatment with TFA in CH2Cl2 according to the general procedure M. Obtained as a eggshell solid (146 mg).
Sources & evidence
- ORD record
- ord-268bfc0d12ce45a48d35faa2f1f9fd0b
- Source dataset
- uspto-grants-2006_12
- Patent number
- US07151098B2
Reaction notes
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