Methyl chloroformate → HCID 59643364, compound

HRID 2251544Notes

Reaction equation

[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]([CH2:26][C:27]2[CH:32]=[CH:31][C:30]([C:33]([F:36])([F:35])[F:34])=[CH:29][CH:28]=2)[CH2:9][CH2:10][C:11]2[CH:25]=[CH:24][C:14]([O:15][C:16]([CH3:23])([CH3:22])[C:17]([O:19]CC)=[O:18])=[CH:13][CH:12]=2)=[N:6][CH:7]=1.[CH3:37][O:38][C:39](Cl)=[O:40]>>[CH3:37][O:38][C:39]([NH:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]([CH2:26][C:27]2[CH:28]=[CH:29][C:30]([C:33]([F:36])([F:34])[F:35])=[CH:31][CH:32]=2)[CH2:9][CH2:10][C:11]2[CH:12]=[CH:13][C:14]([O:15][C:16]([CH3:23])([CH3:22])[C:17]([OH:19])=[O:18])=[CH:24][CH:25]=2)=[N:6][CH:7]=1)=[O:40]

Participants

Reactant 2

HCID 6586Methyl chloroformate

HCID 59643282HCID 59643282, compound

Product 1

HCID 59643364HCID 59643364, compound

Procedure

Similarly prepared from ethyl 2-[4-(2-{(5-aminopyridin-2-yl)[4-(trifluoromethyl)benzyl]amino}ethyl)phenoxy]-2-methylpropanoate and methylchloroformate.

Sources & evidence

ORD record: ord-f09e61af3781419baa8bf7e9b4770a04
Source dataset: uspto-grants-2008_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07319104B2

Reaction notes

Loading…