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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164210Generated: November 2, 2026

Water → HCID 20137751, compound

https://huagongshe.com/reaction/2164210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl (4-methoxy-6-methylpyrimidin-2-yl)carbamateHCID 13072161—
ReactantTrimethylaluminumHCID 16682925—
Reactant2,3-Dihydro-1,4-benzodithiine-5-sulfonamideHCID 20137748—
CatalystHydrochloric AcidHCID 313—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 20137751HCID 20137751—

Reaction Steps

To a solution of 2.5 g 1,4-benzodithian-5-sulfonamide, prepared in Example 18, in 50 ml methylene chloride at ambient temperature under nitrogen is added 5.5 ml trimethylaluminum (2M in toluene). After stirring 15 minutes at ambient temperature 2.0 g of methyl [4-methoxy-6-methylpyrimidin-2-yl]carbamate, prepared according to the procedure of Example 3, is added and the reaction mixture is heated at reflux for 16 hours. The reaction mixture is cooled to ambient temperature and 75 ml water, 10 ml glacial acetic acid, and 10 drops hydrochloric acid are sequentially added. The organic phase is separated, dried, and the solvent removed under reduced pressure to give an oil. Crystallization of the oil from n-butyl chloride/ether gives a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04502882
Source datasetuspto-grants-1985_03
ORD IDord-4e6fb41d7a224b61b95089c0218a07d5
Source noteuspto-grants-1985_03