Trifluoroacetic acid → HCID 18613294, compound
Reaction equation
C(OC(=O)[NH:7][C:8]1[CH:13]=[C:12]([N:14]2[CH2:17][CH2:16][CH2:15]2)[C:11]([Cl:18])=[CH:10][C:9]=1[NH:19][C:20](=[O:32])[CH2:21][C:22]([C:24]1[CH:29]=[CH:28][N:27]=[C:26]([C:30]#[N:31])[CH:25]=1)=O)(C)(C)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[N:14]1([C:12]2[C:11]([Cl:18])=[CH:10][C:9]3[NH:19][C:20](=[O:32])[CH2:21][C:22]([C:24]4[CH:29]=[CH:28][N:27]=[C:26]([C:30]#[N:31])[CH:25]=4)=[N:7][C:8]=3[CH:13]=2)[CH2:17][CH2:16][CH2:15]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound was prepared from {5-azetidin-1-yl-4-chloro-2-[3-(2-cyano-pyridin-4-yl)-3-oxo-propionylamino]-phenyl}-carbamic acid tert. -butyl ester (Example M50) by treatment with TFA in CH2Cl2 according to the general procedure N. Obtained as an orange solid (66 mg).
Sources & evidence
- ORD record
- ord-50bf607ab9a94c61af86ca364fc9730c
- Source dataset
- uspto-grants-2003_04
- Patent number
- US06544985B2
Reaction notes
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