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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356206Generated: November 2, 2026

Benzenesulfonyl chloride → HCID 12069136, compound

https://huagongshe.com/reaction/1356206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantHCID 12069135HCID 12069135—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 12069136HCID 12069136—

Reaction Steps

5-[(2S)-2-Amino-2-(4-methoxy-benzylcarbamoyl)-ethyl]-2-methoxycarbonylmethoxy-benzoic acid methyl ester of Step G (40 mg, 0.072 mmol) is stirred in pyridine (0.5 mL) at 0° C. under N2. Benzenesulfonyl chloride (20 mg, 0.11 mmol) is added and the reaction is stirred overnight at RT. The mixture is then diluted with CH2Cl2 (20 mL), washed with 2N HCl (2×20 mL) and then with saturated NaHCO3 (2×20 mL). The organics are dried over MgSO4, filtered, concentrated and purified by flash column chromatography to provide 5-[(2S)-2-benzenesulfonylamino-2-(4-methoxy-benzylcarbamoyl)-ethyl]-2-methoxycarbonylmethoxy-benzoic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586467B2
Source datasetuspto-grants-2003_07
ORD IDord-7663822e186946278891f037c106bdca
Source noteuspto-grants-2003_07