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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365824Generated: November 1, 2026

Iodine → 4-(5-Chloro-2-iodothiazolo[4,5-d]pyrimidin-7-yl)morpholine

https://huagongshe.com/reaction/1365824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantWaterHCID 962—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactant5-Chloro-7-(morpholin-4-yl)[1,3]thiazolo[4,5-d]pyrimidineHCID 57685414—
SolventTetrahydrofuranHCID 8028—
Product4-(5-Chloro-2-iodothiazolo[4,5-d]pyrimidin-7-yl)morpholineHCID 25252763—

Reaction Conditions

Temperature-50 °C

Reaction Steps

4-(5-Chlorothiazolo[4,5-d]pyrimidin-7-yl)morpholine 16 was dissolved in tetrahydrofuran and iodine (3 eq) was added. The solution was cooled to −50° C. and potassium bis(trimethylsilyl)amide (1.2 eq of 0.5M solution in toluene) was added over a period of 10 minutes. The solution was warmed to room temperature and stirred overnight. Water was added to quench the reaction and the tetrahydrofuran was removed in vacuo. The residue was brought up in methylene chloride, washed with saturated sodium bicarbonate solution and dried with magnesium sulfate. The solution was concentrated a purified by silica gel chromatography to yield 4-(5-chloro-2-iodothiazolo[4,5-d]pyrimidin-7-yl)morpholine 27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893059B2
Source datasetuspto-grants-2011_02
ORD IDord-44f349ba2ee243c3b02d4f72664edf09
Source noteuspto-grants-2011_02