Trifluoroacetic acid → HCID 70225437, compound
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]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
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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