Methyl Lactate → HCID 68566108, compound

HRID 747634Notes

Reaction equation

HRID 747634 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][S:9]([C:12]2[CH:17]=[CH:16][C:15]([O:18][CH3:19])=[C:14]([O:20][CH3:21])[CH:13]=2)(=[O:11])=[O:10])=[C:4]([CH2:22][C:23]2[C:28]([F:29])=[CH:27][CH:26]=[CH:25][C:24]=2[F:30])[CH:3]=1.[C:31]([O:36][CH3:37])(=[O:35])[CH:32]([CH3:34])O>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]([S:9]([C:12]2[CH:17]=[CH:16][C:15]([O:18][CH3:19])=[C:14]([O:20][CH3:21])[CH:13]=2)(=[O:10])=[O:11])[C@H:32]([C:31]([O:36][CH3:37])=[O:35])[CH3:34])=[C:4]([CH2:22][C:23]2[C:28]([F:29])=[CH:27][CH:26]=[CH:25][C:24]=2[F:30])[CH:3]=1

Participants

3

Reactant 2

HCID 11040Methyl LactateHCID 68564783HCID 68564783, compound

Product 1

HCID 68566108HCID 68566108, compound

Procedure

By reaction of 2 g of N-[4-chloro-2-(2,6-difluorobenzyl)phenyl]-3,4-dimethoxybenzenesulfonamide with methyl lactate according to process 35, 1.393 g of the expected product are obtained.

Sources & evidence

ORD record
ord-45fce23137d340639ee42be0c520f5fd
Source dataset
uspto-grants-2008_07
Patent number
US07396958B2

Reaction notes

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