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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032615Generated: November 2, 2026

N-methoxy-N-methylcarbamoyl chloride → HCID 14500904, compound

https://huagongshe.com/reaction/1032615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methoxy-N-methylcarbamoyl chlorideHCID 2734926—
ReactantHCID 14500903HCID 14500903—
SolventPyridineHCID 1049—
ProductHCID 14500904HCID 1450090483.2%

Reaction Steps

2.0 g of 2-(2,3-dihydro-2,2-dimethyl-7-benzofuranylmethyloxy)-5-aminopyridine was dissolved into 5 ml of pyridine, and 1.1 g of N-methoxy-N-methylcarbamoyl chloride was slowly added dropwise thereto under cooling with ice. After 2-hours' continuous stirring, pyridine was distilled off under a reduced pressure, and the residual oily matter was dissolved into 30 ml of toluene. After the mixture was subsequently washed with water, diluted hydrochloric acid and saturated sodium chloride aqueous solution, toluene was distilled off. The residue was subjected to silica gel column chromatography using ethyl acetate/n-hexane (1/1) as a developer to obtain 2.2 g of 1-[2-(2,3-dihydro-2,2-dimethyl-7-benzofuranylmethyloxy)-5-pyridyl]-3-methoxy-3-methylurea.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04959092
Source datasetuspto-grants-1990_09
ORD IDord-a591f3d5c28846d6a6c296acf77f940c
Source noteuspto-grants-1990_09