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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063963Generated: October 31, 2026

Methanol → HCID 23401648, compound

https://huagongshe.com/reaction/1063963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 23401649HCID 23401649—
ProductHCID 23401648HCID 2340164866%

Reaction Steps

To a stirring solution of 4-chloro-N-(2,5-dichlorophenyl)-N-(3-(2-carboxymethyl-3-thiazolidinyl)-1(R)-methylpropyl)benzenesulfonamide (109 mg, 0.203 mmol) in methanol (20 mL) was added 50% aqueous KOH (1.0 mL) and the mixture was stirred at room temperature for 18 hours. The solvent was removed and the crude mixture was dissolved in CH2Cl2 and washed with 1N HCl. The CH2Cl2 layer was dried over Na2SO4 and evaporated to give crude product. Purification was performed over silica gel using 5-10% methanol in CH2Cl2 with 0.5% NH4OH to afford 4-chloro-N-(2,5-dichlorophenyl)-N-(3-(2-carboxy-3-thiazolidinyl)-1(R)-methylpropyl)benzenesulfonamide as a beige foam in 66% yield. IR (KBr) 1467, 1351, 1167, 1094, 753, 622 cm−1; MS (ESI+), 523 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06967196B1
Source datasetuspto-grants-2005_11
ORD IDord-84f3cbc272444add85c33b1b8bcf62d2
Source noteuspto-grants-2005_11