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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719704Generated: November 2, 2026

Sodium borohydride → HCID 20266409, compound

https://huagongshe.com/reaction/1719704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 20266408HCID 20266408—
SolventEthanolHCID 702—
ProductHCID 20266409HCID 20266409—

Reaction Steps

Sodium borohydride (40 mg) was added at 0° to a stirred solution of 2-{2-oxo-2-[1-(6,7-dimethoxyquinazolin-4-yl)piperid-4-yl]ethyl}-5-methyl-1,2,6-thiadiazine-1,1-dioxide (0.4 g) in ethanol (10 cm3). After 2 hours the volatile material was removed in vacuo and the residue was partitioned between water (10 cm3) and dichloromethane (20 cm3). The dried organic extract was evaporated to give a solid which was chromatographed on silica ("Merck" 60.9385) eluting with methanol:chloroform, 1:19, to give a foam which was crystallised from ethyl acetate to afford 2-{2-hydroxy-2-[1-(6,7-dimethoxyquinazolin-4-yl)piperid-4-yl]ethyl}-5-methyltetrahydro-1,2,6-thiadiazine-1,1-dioxide as microcrystals, m.p. 189°-193° (0.30 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04542132
Source datasetuspto-grants-1985_09
ORD IDord-25ba1cfb4dcd4dbd835938ce7afebb7a
Source noteuspto-grants-1985_09