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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365829Generated: October 31, 2026

Dichloromethane → 5-Chloro-2-(methylsulfonyl)-7-morpholinothiazolo[4,5-d]pyrimidine

https://huagongshe.com/reaction/1365829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium hydroxy sulfiteHCID 23707502—
ReactantHCID 57685391HCID 57685391—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product5-Chloro-2-(methylsulfonyl)-7-morpholinothiazolo[4,5-d]pyrimidineHCID 57685406—

Reaction Conditions

Temperature50 °C

Reaction Steps

5-Chloro-2-(methylthio)-7-morpholinothiazolo[4,5-d]pyrimidine was dissolved in methanol. Oxone (2.2 eq) was added in water (10:1 ratio methanol:water). The solution was heated to 50° C. for 2.5 hours. One additional equivalent of oxone was added (if needed) and solution was stirred at 50° C. for an additional 1 hour. The solution was cooled to room temperature and methylene chloride was added. The resulting solid was filtered off and rinsed with methylene chloride. The organic solution was washed with saturated sodium bicarbonate solution (pH test neutral), dried with magnesium sulfate and concentrated to yield 5-chloro-2-(methylsulfonyl)-7-morpholinothiazolo[4,5-d]pyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893059B2
Source datasetuspto-grants-2011_02
ORD IDord-2ef79c6f1c79499693b87bf552797b0f
Source noteuspto-grants-2011_02