Trifluoroacetic acid → HCID 178440668, compound

HRID 22052Notes

Reaction equation

HRID 22052 reaction equation
[CH2:1]([C:5]1[N:13]2[C:8]([C:9](=[CH:31][C:32]([O:34]C(C)(C)C)=[O:33])[CH2:10][CH2:11][CH:12]2[C:14]2[CH:19]=[CH:18][C:17]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=3[C:26]3[NH:30][N:29]=[N:28][N:27]=3)=[CH:16][CH:15]=2)=[CH:7][CH:6]=1)[CH2:2][CH2:3][CH3:4].C(O)(C(F)(F)F)=O>>[CH2:1]([C:5]1[N:13]2[C:8]([C:9](=[CH:31][C:32]([OH:34])=[O:33])[CH2:10][CH2:11][CH:12]2[C:14]2[CH:19]=[CH:18][C:17]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=3[C:26]3[NH:27][N:28]=[N:29][N:30]=3)=[CH:16][CH:15]=2)=[CH:7][CH:6]=1)[CH2:2][CH2:3][CH3:4]

Participants

3

Procedure

To a solution of unsaturated tert-butyl ester (0.0627 mmol, the title compound of Example 1924) in 2 mL of CDCl3 at room temperature is added 0.5 mL of TFA, and the progress of the reaction is monitored by 1H NMR. The resulting yellow solution is stirred at room temperature until the reaction is complete. The mixture is concentrated in vacuo. The crude product is purified to give the title compound of Example 1925.

Workup

  1. concentrationThe mixture is concentrated in vacuo
  2. customThe crude product is purified

Sources & evidence

ORD record
ord-7cad0f1facf145ee9f0d98ea6e49be98
Source dataset
uspto-grants-1995_06
Patent number
US05426105

Reaction notes

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