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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981269Generated: November 1, 2026

2-Amino-4,6-dimethyl pyrimidine → N-[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]-2,3-dihydro-2,2-dimethyl-7-benzofuransulfonamide

https://huagongshe.com/reaction/1981269

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4,6-dimethyl pyrimidineHCID 13021—
Reactant2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-sulfonyl isocyanateHCID 13424182—
SolventTetrahydrofuranHCID 8028—
ProductN-[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]-2,3-dihydro-2,2-dimethyl-7-benzofuransulfonamideHCID 1342418354.5%

Reaction Steps

To a solution of 1.2 g of 2-amino-4,6-dimethylpyrimidine in 25 ml of tetrahydrofuran was added 2.5 g of 2,3-dihydro-2,2-dimethyl-7-benzofuransulfonyl isocyanate prepared above. After a slight exotherm the solution was stirred at room temperature for 4 hours. The solution was concentrated in vacuo to give a viscous oil that precipitated a solid from 10 ml of acetonitrile. The solid was recrystallized from acetonitrile to give 2 g of N-[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]-2,3-dihydro-2,2-dimethyl-7-benzofuransulfonamide, m.p. 203°-206° C. The IR spectrum showed a carbonyl absorption at 1680 cm-1 indicative of a sulfonylurea.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04514211
Source datasetuspto-grants-1985_04
ORD IDord-2c877a6f1c2846b8b78213b42efd28c5
Source noteuspto-grants-1985_04