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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2058105Generated: November 2, 2026

Benzenesulfonyl isocyanate, 2-chloro- → HCID 13469506, compound

https://huagongshe.com/reaction/2058105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl isocyanate, 2-chloro-HCID 174071—
ReactantHCID 3777900HCID 3777900—
SolventDichloromethaneHCID 6344—
ProductHCID 13469506HCID 13469506—

Reaction Steps

To a dry stirred solution of 18.3 parts of 2-amino-4-(2-methoxyethoxy)-6-methylpyrimidine in 300 parts of methylene chloride at ambient temperature and pressure was added 22 parts of 2-chlorobenzenesulfonylisocyanate. The mixture was stirred for 2 hours and then the methylene chloride was removed under reduced pressure. The resulting solid was triturated with 1-chlorobutane and filtered to yield 35 parts of N-[[4-(2-methoxyethoxy)-6-methylpyrimidine-2-yl]aminocarbonyl]-2-chlorobenzenesulfonamide, m.p. 130°-140° C. The product showed characteristic absorption bands in the infrared spectrum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04214890
Source datasetuspto-grants-1980_07
ORD IDord-4aa073ce5363403e8edc0ae48369e9a6
Source noteuspto-grants-1980_07