Methyl chloroformate → HCID 86720660, compound

HRID 2201867Notes

Reaction equation

HRID 2201867 reaction equation
[NH2:1][C:2]1[CH:7]=[C:6]([Cl:8])[C:5]([C:9]([N:11]2[C:19]3[CH:18]=[CH:17][N:16]=[CH:15][C:14]=3[CH:13]=[CH:12]2)=[O:10])=[C:4]([Cl:20])[CH:3]=1.[CH3:21][O:22][C:23](Cl)=[O:24].COC(=O)NC1C2C=CN(C(=O)C3C(Cl)=CC=CC=3Cl)C=2C=CN=1>>[CH3:21][O:22][C:23](=[O:24])[NH:1][C:2]1[CH:3]=[C:4]([Cl:20])[C:5]([C:9]([N:11]2[C:19]3[CH:18]=[CH:17][N:16]=[CH:15][C:14]=3[CH:13]=[CH:12]2)=[O:10])=[C:6]([Cl:8])[CH:7]=1

Participants

4

Procedure

Methyl[3,5-dichloro-4-(1H-pyrrolo[3,2-c]pyridin-1-ylcarbonyl)phenyl]carbamate (Compound No. 79) was prepared by treating (4-amino-2,6-dichlorophenyl)(1H-pyrrolo[3,2-c]pyridin-1-yl)methanone with methylchloroformate following a procedure similar to the one used for methyl[1-(2,6-dichlorobenzoyl)-1H-pyrrolo[3,2-c]pyridin-4-yl]carbamate (Compound No. 74).

Sources & evidence

ORD record
ord-5c762cc3b226482aa172e8062975dfa7
Source dataset
uspto-grants-2016_06
Patent number
US09364466B2

Reaction notes

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