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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121718Generated: November 2, 2026

Pyridine → HCID 23434125, compound

https://huagongshe.com/reaction/2121718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Reactant2,5-Dichlorothiophene-3-carbonyl chlorideHCID 2777084—
SolventDichloromethaneHCID 6344—
ProductHCID 23434125HCID 2343412591%

Reaction Steps

To a stirred solution of 2,5-dichloro-3-thiophenecarbonylchloride (1.08 g, 5.0 mmol) and pyridine (2 mL) in CH2Cl2 (10 mL) was added N,O-dimethylhydroxylamine hydrochloride (490 mg, 5.0 mmol) at room temperature, and the mixture was stirred for 18 hours. CH2Cl2 (10 mL) was added to the mixture. The combined organic layers were washed with 1N HCl solution, saturated NaHCO3 solution, brine, dried over MgSO4, and concentrated in vacuo to give light yellow oil (1.09 g, 91% yield). The compound was used for next reaction without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696470B2
Source datasetuspto-grants-2004_02
ORD IDord-b3083efe014040728a2a615d0b7e48e0
Source noteuspto-grants-2004_02