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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591249Generated: October 30, 2026

Triethylamine → 3-[(-)-camphanoyl]-5-[1-(3,4-methylenedioxybenzoyl)-1,2,3, 4-tetrahydroquinol-6-yl]-6-methyl-3,6-dihydro-2H-1,3,4-thiadiazin-2-one

https://huagongshe.com/reaction/1591249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-[1-(3,4-methylenedioxybenzoyl)-1,2,3, 4-tetrahydroquinol-6-yl]-6-methyl-3,6-dihydro-2H-1,3,4-thiadiazin-2-oneHCID 11825724—
Reactant4,7,7-Trimethyl-3-bicyclo[2.2.1]heptanecarbonyl chlorideHCID 53442783—
SolventDichloromethaneHCID 6344—
Product3-[(-)-camphanoyl]-5-[1-(3,4-methylenedioxybenzoyl)-1,2,3, 4-tetrahydroquinol-6-yl]-6-methyl-3,6-dihydro-2H-1,3,4-thiadiazin-2-oneHCID 67884999—

Reaction Steps

A solution of 26 g of (-)-camphanic acid chloride in 100 ml of methylene chloride is added dropwise at 0°, with stirring, to a suspension of 48 g of 5-[1- (3,4-methylenedioxybenzoyl)-1,2,3, 4-tetrahydroquinol-6- yl]-6-methyl-3,6-dihydro-2H-1,3,4-thiadiazin-2-one in 800 ml of methylene chloride to which 20 ml of triethylamine have been added, and the reaction mixture is stirred for 4 hours. It is then washed with dilute hydrochloric acid and subsequently with bicarbonate solution. The organic phase is separated off and worked up in conventional manner to give 3-[(-)-camphanoyl]-5-[1-(3,4-methylenedioxybenzoyl)-1,2,3, 4- tetrahydroquinol-6-yl]-6-methyl-3,6-dihydro-2H-1,3,4- thiadiazin-2-one as a mixture of diastereoisomers, m.p. 216°-217° .

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05206363
Source datasetuspto-grants-1993_04
ORD IDord-a19d865a2478427c977140d5abb19f6d
Source noteuspto-grants-1993_04