Ethyl chloroformate → HCID 59536793, compound
Reaction equation
[NH2:1][CH2:2][CH:3]([NH:12][C:13](=[O:19])[O:14][C:15]([CH3:18])([CH3:17])[CH3:16])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([Cl:10])[C:5]=1[Cl:11].Cl[C:21]([O:23][CH2:24][CH3:25])=[O:22]>>[Cl:11][C:5]1[C:6]([Cl:10])=[CH:7][CH:8]=[CH:9][C:4]=1[CH:3]([NH:12][C:13](=[O:19])[O:14][C:15]([CH3:16])([CH3:18])[CH3:17])[CH2:2][NH:1][C:21](=[O:22])[O:23][CH2:24][CH3:25]Participants
3
Procedure
From 192 mg (629 μmol) of the compound from Example 40A and 72 μl (755 μmol) of ethyl chloroformate, in the same way as for Example 123A, 184 mg (78% of theory) of the title compound were prepared.
Sources & evidence
- ORD record
- ord-e41dd288bfe142f7a2ada45ba82decfa
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08796324B2
Reaction notes
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