Trifluoroacetic acid → 2-[7-(2-Fluoro-phenyl)-4-oxo-4,5-dihydro-1H-benzo[b][1,4]diazepin-2-yl]-thiophene-3-carbonitrile

HRID 859544Notes

Reaction equation

HRID 859544 reaction equation
C(OC(=O)[NH:7][C:8]1[CH:13]=[CH:12][C:11]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=2[F:20])=[CH:10][C:9]=1[NH:21][C:22](=[O:33])[CH2:23][C:24]([C:26]1[S:27][CH:28]=[CH:29][C:30]=1[C:31]#[N:32])=O)(C)(C)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[F:20][C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][C:14]=1[C:11]1[CH:12]=[CH:13][C:8]2[NH:7][C:24]([C:26]3[S:27][CH:28]=[CH:29][C:30]=3[C:31]#[N:32])=[CH:23][C:22](=[O:33])[NH:21][C:9]=2[CH:10]=1

Participants

4

Procedure

Prepared from {3-[3-(3-cyano-thiophen-2-yl)-3-oxo-propionylamino]-2′-fluoro-biphenyl-4-yl}-carbamic acid tert.-butyl ester (Example K55) by treatment with TFA in CH2Cl2 according to the general procedure M. Obtained as a yellow solid (258 mg).

Sources & evidence

ORD record
ord-8f03b9c5d99143b5b650df8ca4ff7516
Source dataset
uspto-grants-2006_12
Patent number
US07151098B2

Reaction notes

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