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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542688Generated: October 26, 2026

Water → N-[(4-Methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]-1,4-benzodioxan-5-sulfonamide

https://huagongshe.com/reaction/542688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl (4-methoxy-6-methylpyrimidin-2-yl)carbamateHCID 13072161—
Reactant2,3-Dihydro-1,4-benzodioxine-5-sulfonamideHCID 13455428—
ReactantTrimethylaluminumHCID 16682925—
CatalystHydrochloric AcidHCID 313—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductN-[(4-Methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]-1,4-benzodioxan-5-sulfonamideHCID 13455430—

Reaction Steps

To a solution of 1.0 g 1,4-benzodioxan-5-sulfonamide, prepared in Example 15, in 50 ml methylene chloride at ambient temperature under nitrogen was added 2.5 ml trimethylaluminum (2M in toluene). After stirring 15 minutes at ambient temperature, 1.0 g of methyl[4-methoxy-6-methylpyrimidin-2-yl]carbamate, prepared according to the procedure of Example 3, was added and the reaction mixture was heated at reflux for 72 hours. The reaction mixture was cooled to ambient temperature and 75 ml water, 10 ml glacial acetic acid and 10 drops hydrochloric acid were sequentially added. The organic phase was separated, dried, and the solvent removed under reduced pressure to give an oil. Crystallization of the oil from n-butyl chloride/ether gave a solid, m.p. 203°-205° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04659368
Source datasetuspto-grants-1987_04
ORD IDord-28d558f51c7d45fb9884936b786897c0
Source noteuspto-grants-1987_04