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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925707Generated: October 24, 2026

Methyl 3-amino-2-thiophenecarboxylate → Methyl 3-(4-tert-butylphenylsulfonamido)thiophene-2-carboxylate

https://huagongshe.com/en/reaction/1925707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-amino-2-thiophenecarboxylateHCID 89652—
Reactant4-t-Butylbenzenesulfonyl chlorideHCID 139882—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-(4-tert-butylphenylsulfonamido)thiophene-2-carboxylateHCID 801564366%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of methyl 3-aminothiophene-2-carboxylate (0.55 g; 3.5 mmol) in pyridine (2 mL) and dichloromethane (2 mL) was added 4-tert-butylbenzenesulfonyl chloride (0.98 g; 4.2 mmol). The resulting mixture was warmed to 40° C. to aid in solubility, then stirred at room temperature for 48 hours. The reaction mixture was diluted with dichloromethane and washed with aqueous hydrochloric acid (2N). The aqueous layer was separated and extracted with dichloromethane. The organic layers were combined, dried over anhydrous sodium sulfate, decanted, and filtered through a and of silica. The silica was washed with dichloromethane. The eluant was combined with hexanes and allowed to stand. After 24 hours the resulting solid product was collected by filtration to give the desired product as a white solid (817 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178699B2
Source datasetuspto-grants-2012_05
ORD IDord-4fc1342cfdfe4611b700d4c23e1bcb89
Source noteuspto-grants-2012_05