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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328202Generated: October 30, 2026

N-Acetylsulfanilyl chloride → HCID 86734626, compound

https://huagongshe.com/reaction/328202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Acetylsulfanilyl chlorideHCID 8481—
ReactantHCID 21444304HCID 21444304—
SolventPyridineHCID 1049—
ProductHCID 86734626HCID 86734626—

Reaction Steps

A mixture of 10.6 g. of 1-cyclopropylcytosine, 16.4 g. of N-acetylsulfanilyl chloride and 47 ml. of pyridine was stirred overnight after momentary cooling to maintain the reaction below 30°. The mixture was poured into 700 ml. of water, and after filtration by gravity, the solution was strongly acidified by addition of 6N hydrochloric acid. Gradual crystallization occurred overnight in a refrigerator before filtering the N4 -acetyl-N1 -(1-cyclopropyl-1,2-dihydro-2-oxo-4-pyrimidinyl)-sulfanilamide; yield 10.7 g., m.p. 139°-143°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04016267
Source datasetuspto-grants-1977_04
ORD IDord-fee3259df9034774a0248d88d966ef8a
Source noteuspto-grants-1977_04