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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110015Generated: November 2, 2026

Pyridine → HCID 69063936, compound

https://huagongshe.com/reaction/2110015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-Nitrobenzenesulfonyl chlorideHCID 15540—
ReactantMethyl 3-amino-4-[(tert-butoxycarbonyl)amino]benzoateHCID 18621647—
SolventDichloromethaneHCID 6344—
ProductHCID 69063936HCID 69063936—

Reaction Steps

After dissolving 3-amino-4-tert-butoxycarbonylaminobenzoic acid methyl ester (817.3 mg, 3.07 mmol) in dichloromethane (10 ml), pyridine (0.373 ml, 4.60 mmol) and 2-nitrobenzenesulfonyl chloride (815 mg, 3.68 mmol) were added in an ice bath, and the mixture was stirred at room temperature for 4 hours. Pyridine (0.050 ml) and 2-nitrobenzenesulfonyl chloride (135 mg) were added, and stirring was continued for 2 hours. The reaction mixture was concentrated under reduced pressure, water (30 ml) was added, and then extraction was performed with ethyl acetate (20 ml×3 times). The obtained organic layer was washed with saturated brine and then dried over anhydrous magnesium sulfate. After concentration under reduced pressure, the crystallized residue was suspended in n-hexane-ethyl acetate (4:1), filtered, and dried to obtain 4-tert-butoxycarbonylamino-3-(2-nitro-benzenesulfonylamino)-benzoic acid methyl ester. The compound was identified by LC-MS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517875B2
Source datasetuspto-grants-2009_04
ORD IDord-8f950a557c6748329d431bf03c815f56
Source noteuspto-grants-2009_04