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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719705Generated: November 3, 2026

Sodium hydride → HCID 20266398, compound

https://huagongshe.com/reaction/1719705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1,3-PropanesultamHCID 642157—
ReactantHCID 20266386HCID 20266386—
SolventDimethylformamideHCID 6228—
ProductHCID 20266398HCID 20266398—

Reaction Steps

Sodium hydride (1.25 g of a 50% dispersion in oil) was added at room temperature to a stirred solution of isothiazolidine-1,1-dioxide (2.42 g) in DMF (15 cm3). After stirring for 0.5 hours 2-methyl-2-[1-(6,7-dimethoxyquinazolin-4-yl)piperid-4-yl]oxirane (5.0 g) was added and the mixture was stirred for 4 hours at 100°. Volatile material was removed in vacuo, the residue was partitioned between chloroform (100 cm3) and water (50 cm3) and the chloroform layer was dried (MgSO4) and evaporated. The residue was chromatographed on silica ("Merck" 60.9385) eluting with methanol:ethyl acetate, 1:4, to give a solid which was recrystallised from ethyl acetate-methanol to give 2-{2-hydroxy-2-[1-(6,7-dimethoxyquinazolin-4-yl)piperid-4-yl]prop-1-yl}isothiazolidine-1,1-dioxide, m.p. 173°-174° (4.15 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04542132
Source datasetuspto-grants-1985_09
ORD IDord-0ac898f11f384d3ab3f3ae727bbdc046
Source noteuspto-grants-1985_09