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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351855Generated: November 1, 2026

Water → HCID 136364555, compound

https://huagongshe.com/reaction/2351855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 136364556HCID 136364556—
SolventTetrahydrofuranHCID 8028—
ProductHCID 136364555HCID 136364555—

Reaction Steps

In an argon stream, 630 mg (1.68 mM) of ethyl 3-hydroxymethyl-6-methyl-4-(3-nitrophenyl)-4,7-dihydroisothiazolo[5,4-b]pyridine-5-carboxylate obtained in Example 2 was dissolved in 6 ml of anhydrous tetrahydrofuran, and under ice cooling, 0.62 ml (4.45 mM) of triethylamine was added. A solution of 0.26 ml (3.36 mM) of methanesulfonyl chloride in 2 ml of anhydrous tetrahydrofuran was added dropwise, and reacted at the above temperature for 45 minutes. Water (6 ml) was added to the reaction mixture, and the mixture was stirred for 10 minutes. The mixture was then poured into 10% HCl-ice, and extracted with methylene chloride. The methylene chloride layer was washed with water and a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give 927 mg of crude ethyl 3-methanesulfonyloxymethyl-6-methyl-4-(3-nitrophenyl)-4,7-dihydroisothiazolo[5,4-b]pyridine-5-carboxylate as a pale yellow jelly-like product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04874760
Source datasetuspto-grants-1989_10
ORD IDord-c194f374211644158925a3dcb2a66263
Source noteuspto-grants-1989_10