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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 972402Generated: October 26, 2026

4-Bromo-2-methylphenyl isocyanate → tetrahydro-1-(5-methylsulfinyl-1,3,4-thiadiazol-2-yl)-3-propargyl-6-[N-(2-methyl-4-bromophenyl)carbamoyloxy]-2(1H)-pyrimidinone

https://huagongshe.com/reaction/972402

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-methylphenyl isocyanateHCID 2735594—
Reactanttetrahydro-1-(5-methylsulfinyl-1,3,4-thiadiazol-2-yl)-3-propargyl-6-hydroxy-2(1H)-pyrimidinoneHCID 21400073—
CatalystTriethylamineHCID 8471—
Producttetrahydro-1-(5-methylsulfinyl-1,3,4-thiadiazol-2-yl)-3-propargyl-6-[N-(2-methyl-4-bromophenyl)carbamoyloxy]-2(1H)-pyrimidinoneHCID 21404013—

Reaction Steps

Tetrahydro-1-(5-methylsulfinyl-1,3,4-thiadiazol-2-yl)-3-propargyl-6-hydroxy-2(1H)-pyrimidinone (0.05 mole) and 2-methyl-4-bromophenyl isocyanate (3.5 ml; 0.06 mole) are charged into a glass reaction vessel equipped with a mechanical stirrer. The mixture is stirred and triethylamine (1 drop) is added thereto. After the addition is completed the reaction mixture is allowed to stand for a period of about 1 hour. The mixture is then washed with hexane and is dried to yield the desired product tetrahydro-1-(5-methylsulfinyl-1,3,4-thiadiazol-2-yl)-3-propargyl-6-[N-(2-methyl-4-bromophenyl)carbamoyloxy]-2(1H)-pyrimidinone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04053298
Source datasetuspto-grants-1977_10
ORD IDord-7cb6c9e219a74cd5aed59dbc0d5daeb3
Source noteuspto-grants-1977_10