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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482797Generated: October 30, 2026

2-Amino-4,6-dimethoxypyrimidine → N-[(4,6-Dimethoxypyrimidin-2-yl)aminocarbonyl]-2-(dimethylaminosulfonyloxy)benzenesulfonamide

https://huagongshe.com/reaction/482797

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4,6-dimethoxypyrimidineHCID 118946—
Reactant2-(Dimethylaminosulfonyloxy)benzenesulfonyl isocyanateHCID 13473127—
SolventDichloromethaneHCID 6344—
ProductN-[(4,6-Dimethoxypyrimidin-2-yl)aminocarbonyl]-2-(dimethylaminosulfonyloxy)benzenesulfonamideHCID 1347312886.7%

Reaction Steps

To a suspension of 0.46 g (0.003 mole) 2-amino-4,6-dimethoxypyrimidine in 5 ml methylene chloride was added 1.2 g (0.004 mole) 2-(dimethylaminosulfonyloxy)-benzenesulfonyl isocyanate. The reaction exothermed (18°-26° C.) and was then stirred at room temperature 3 hours. The solvent was evaporated under reduced pressure. The resultant mixture was triturated with diethyl ether and filtered to give 1.2 g of a white solid, m.p. 165°-168° C. The infrared spectrum shows absorption bands at 1710, 1380, 1170 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04576633
Source datasetuspto-grants-1986_03
ORD IDord-1a74b1b6e955422ea447d64bb301bce6
Source noteuspto-grants-1986_03