Trifluoroacetic acid → HCID 178441907, compound

HRID 22056Notes

Reaction equation

HRID 22056 reaction equation
[CH2:1]([C:5]1[N:9]2[CH:10]([C:22]3[CH:27]=[CH:26][C:25]([C:28]4[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=4[C:34]4[NH:38][N:37]=[N:36][N:35]=4)=[CH:24][CH:23]=3)[CH2:11][CH2:12][C:13](=[CH:14][C:15]([O:17]C(C)(C)C)=[O:16])[C:8]2=[N:7][N:6]=1)[CH2:2][CH2:3][CH3:4].C(O)(C(F)(F)F)=O>>[CH2:1]([C:5]1[N:9]2[CH:10]([C:22]3[CH:27]=[CH:26][C:25]([C:28]4[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=4[C:34]4[NH:38][N:37]=[N:36][N:35]=4)=[CH:24][CH:23]=3)[CH2:11][CH2:12][C:13](=[CH:14][C:15]([OH:17])=[O:16])[C:8]2=[N:7][N: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 3229) 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 3230.

Workup

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

Sources & evidence

ORD record
ord-d16391185f414e53af4b1f56e0627ed0
Source dataset
uspto-grants-1995_06
Patent number
US05426105

Reaction notes

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