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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466913Generated: October 29, 2026

Methanesulfonamide → HCID 67831691, compound

https://huagongshe.com/reaction/466913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonamideHCID 72879—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 14853399HCID 14853399—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67831691HCID 6783169158.6%

Reaction Steps

To a solution of 1,1-carbonyldiimidazole (1.70 g, 0.0105 mol) in dry tetrahydrofuran (130 ml), 2-(4,6-dimethoxypyrimidin-2-yl)oxypropionic acid (2.28 g, 0.01 mol), prepared as described in Example 1(b) above, in tetrahydrofuran (30 ml) was added dropwise at room temperature (~20° C.). The solution was refluxed for 1/2 hour and allowed to cool. Methanesulphonamide (0.95 g, 0.01 mol) was added in one solid portion and the mixture stirred for 15 minutes before 1,8-diazabicyclo[5.4.0]undec-7-ene (1.52 g, 0.01 mol) in tetrahydrofuran (30 ml) was added dropwise at room temperature (~20° C.). After a short duration the tetrahydrofuran was removed and the residue acidified with IM hydrochloric acid solution. The product was extracted with chloroform, backwashed with water and dried. The solvent was removed and the product purified on silica gel eluting with 3% by volume methanol/chloroform to yield the title compound as a solid (1.79 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05158599
Source datasetuspto-grants-1992_10
ORD IDord-e44d0f8767de49e9a1565e972c554ae3
Source noteuspto-grants-1992_10