Trifluoroacetic acid → HCID 70225437, compound

HRID 636803Notes

Reaction equation

HRID 636803 reaction equation
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([CH2:14][N:15]2[C:19](=[O:20])[C:18]([CH2:28][C:29]3[CH:34]=[CH:33][N:32]=[CH:31][CH:30]=3)([CH2:21][C:22]3[CH:27]=[CH:26][N:25]=[CH:24][CH:23]=3)[NH:17][C:16]2=[CH:35][C:36]([C:38]2[CH:43]=[CH:42][C:41]([C:44]#[N:45])=[CH:40][CH:39]=2)=[O:37])[CH2:10][CH2:9]1)=O)(C)(C)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[O:20]=[C:19]1[N:15]([CH2:14][CH:11]2[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]2)[C:16](=[CH:35][C:36]([C:38]2[CH:39]=[CH:40][C:41]([C:44]#[N:45])=[CH:42][CH:43]=2)=[O:37])[NH:17][C:18]1([CH2:21][C:22]1[CH:27]=[CH:26][N:25]=[CH:24][CH:23]=1)[CH2:28][C:29]1[CH:34]=[CH:33][N:32]=[CH:31][CH:30]=1

Participants

4

Procedure

Using the same procedure as described in Example 3, the title compound of 40A (0.958 g, 1.58 mmol) was treated with TFA (3 ml) in CH2Cl2 to give the title compound of 40B (0.621 g, 1.23 mmol, 78% yield).

Sources & evidence

ORD record
ord-19ff37683aa04675a75a97d377df68c0
Source dataset
uspto-grants-2001_02
Patent number
US06194438B1

Reaction notes

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