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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925749Generated: October 30, 2026

Pyridine → HCID 59180384, compound

https://huagongshe.com/reaction/1925749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethyl 3-amino-2-thiophenecarboxylateHCID 89652—
ReactantHCID 59180443HCID 59180443—
SolventDichloromethaneHCID 6344—
ProductHCID 59180384HCID 59180384—

Reaction Steps

To a solution of 4-cyclopentyl-2-fluorobenzene-1-sulfonyl chloride, 134 (0.06 g; 0.21 mmol) in dichloromethane (1 mL) at room temperature, methyl 3-aminothiophene-2-carboxylate (0.033 g; 0.21 mmol) was added followed by pyridine (0.033 g; 0.42 mmol) and then stirred at room temperature under a nitrogen atmosphere for 24 hours. The reaction mixture was concentrated under reduced pressure and then taken up in ethyl acetate (10 mL) and washed with water. The aqueous layer was separated and extracted with ethyl acetate (2×10 mL). The combined organic phases were successively washed with water and aqueous saturated sodium chloride, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The resulting crude residue was purified by automated silica gel column chromatography (Biotage®) eluting with ethyl acetate/hexanes (0 to 40% v/v over 900 mL gradient elution) to give the title product as an off-white solid (34 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178699B2
Source datasetuspto-grants-2012_05
ORD IDord-b38a3610001b49d7ad6e1df684925370
Source noteuspto-grants-2012_05