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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063966Generated: November 1, 2026

Potassium Hydroxide → HCID 23401681, compound

https://huagongshe.com/reaction/1063966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantPotassium BromideHCID 253877—
ReactantHCID 23401648HCID 23401648—
ReactantHCID 23401682HCID 23401682—
ProductHCID 23401681HCID 2340168145%

Reaction Steps

4-chloro-N-(2,5-dichlorophenyl)-N-(4-(5-carboxy-3-thiazolidinyl)-1(R)-methylbutyl)benzenesulfonamide was prepared analogous to 4-chloro-N-(2,5-dichlorophenyl)-N-(3-(2-carboxy-3-thiazolidinyl)-1(R)-methylpropyl)benzenesulfonamide by reacting 4-chloro-N-(2,5-dichlorophenyl)-N-(4-(5-carboxymethyl-3-thiazolidinyl)-1(R)-methylbutyl)benzenesulfonamide with 50% aqueous KOH. Yield=45%; White powder: IR (KBr) 1467, 1350, 1167, 1094, 754, 622 cm−1; MS (ESI+), 537 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06967196B1
Source datasetuspto-grants-2005_11
ORD IDord-d003eeb4a4704597beb68dd4f7ec2e19
Source noteuspto-grants-2005_11