Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365777Generated: November 4, 2026

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

https://huagongshe.com/reaction/1365777

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant5-Chloro-7-(morpholin-4-yl)[1,3]thiazolo[4,5-d]pyrimidineHCID 57685414—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product4-(5-Chloro-2-iodothiazolo[4,5-d]pyrimidin-7-yl)morpholineHCID 25252763—

Reaction Conditions

Temperature-40 °C

Reaction Steps

Following the procedures in U.S. Pat. No. 6,492,383, 2.5 M of n-butyllithium (9.4 mL, 22.48 mmol) in hexane solution was added to a mixture of 4-(5-chlorothiazolo[4,5-d]pyrimidin-7-yl)morpholine 16 (3.0 g, 11.74 mmol) in 60 mL of THF at −78° C. The reaction mixture was allowed to warm to −40° C. and stirred for 30 min. A solution of iodine (6.0 g, 23.48 mmol) in 10 mL of THF was added dropwise. After the addition was completed. The reaction mixture was brought to room temperature and stirred for 2 h. The mixture was quenched by diluting with dichloromethane and extracting with H2O (2×100 mL). The organic layer was washed with Na2S2O3 (2×100 mL), H2O (2×100 mL), dried over MgSO4, filtered and evaporated to afford 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-b0e8e86bd5184299816b68c58824947f
Source noteuspto-grants-2011_02