Trifluoroacetic acid → HCID 18613329, compound

HRID 1265847Notes

Reaction equation

HRID 1265847 reaction equation
C(OC(=O)[NH:7][C:8]1[CH:13]=[C:12]([N:14]([CH2:17][CH3:18])[CH2:15][CH3:16])[C:11]([C:19]#[N:20])=[CH:10][C:9]=1[NH:21][C:22](=[O:38])[CH2:23][C:24]([C:26]1[CH:31]=[CH:30][CH:29]=[C:28]([C:32]2[O:36][N:35]=[C:34]([CH3:37])[CH:33]=2)[CH:27]=1)=O)(C)(C)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[CH2:15]([N:14]([CH2:17][CH3:18])[C:12]1[C:11]([C:19]#[N:20])=[CH:10][C:9]2[NH:21][C:22](=[O:38])[CH2:23][C:24]([C:26]3[CH:31]=[CH:30][CH:29]=[C:28]([C:32]4[O:36][N:35]=[C:34]([CH3:37])[CH:33]=4)[CH:27]=3)=[N:7][C:8]=2[CH:13]=1)[CH3:16]

Participants

4

Reactant 2

HCID 6422Trifluoroacetic acidHCID 86586877HCID 86586877, compound

Product 1

HCID 18613329HCID 18613329, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

The title compound was prepared from (4-cyano-5-diethylamino-2-{3-[3-(3-methyl-isoxazol-5-yl)-phenyl]-3-oxo-propionylamino}-phenyl)-carbamic acid tert-butyl ester (Example M94) (0.35 g, 0.66 mmol) by treatment with TFA in CH2Cl2 according to the general procedure N. Obtained as a yellow solid (209 mg, 77%).

Sources & evidence

ORD record
ord-10bfed8dca074c95b45640d5e654c349
Source dataset
uspto-grants-2003_04
Patent number
US06544985B2

Reaction notes

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