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Benzenesulfonyl chloride → [4-Chloro-2-[[3-methyl-4-(phenylsulfonyl)-1-piperazinyl]methyl]phenoxy]acetic Acid

HRID 38267
Notes
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Reaction equation

HRID 38267 reaction equation
[Cl:1][C:2]1[CH:12]=[CH:11][C:5]([O:6][CH2:7][C:8]([OH:10])=[O:9])=[C:4]([CH2:13][N:14]2[CH2:19][CH2:18][N:17]([S:20]([CH2:23][C:24]3[CH:29]=[CH:28][CH:27]=[CH:26]C=3)(=[O:22])=[O:21])[CH:16]([CH3:30])[CH2:15]2)[CH:3]=1.C1(S(Cl)(=O)=O)C=CC=CC=1>>[Cl:1][C:2]1[CH:12]=[CH:11][C:5]([O:6][CH2:7][C:8]([OH:10])=[O:9])=[C:4]([CH2:13][N:14]2[CH2:19][CH2:18][N:17]([S:20]([C:23]3[CH:26]=[CH:27][CH:28]=[CH:29][CH:24]=3)(=[O:21])=[O:22])[CH:16]([CH3:30])[CH2:15]2)[CH:3]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 7369Benzenesulfonyl chlorideHCID 11669635[4-Chloro-2-[[3-methyl-4-[(phenylmethyl]sulfonyl)-1-piperazinyl]methyl]phenoxy]acetic Acid

Product 1

HCID 11655069[4-Chloro-2-[[3-methyl-4-(phenylsulfonyl)-1-piperazinyl]methyl]phenoxy]acetic Acid

Procedure

Prepared by the method of example 30, using the product from example 56 part (a) and is benzenesulfonyl chloride to give the title compound.

Workup

  1. customPrepared by the method of example 30

Sources & evidence

ORD record
ord-a876609625a94e64a22f39f164b58057
Source dataset
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08524715B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes