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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390807Generated: October 30, 2026

Iodine → 4-(2-Chloro-6-iodothieno[3,2-d]pyrimidin-4-yl)morpholine

https://huagongshe.com/reaction/390807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant2-Chloro-4-(morpholin-4-yl)thieno(3,2-d)pyrimidineHCID 20284971—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product4-(2-Chloro-6-iodothieno[3,2-d]pyrimidin-4-yl)morpholineHCID 5959306175.9%

Reaction Conditions

Temperature-40 °C

Reaction Steps

Following the procedures in U.S. Pat. No. 6,492,383, 2.5 M of n-Butylithium (9.4 mL, 22.48 mmol) in hexane solution was added to a mixture of 2-chloro-4-morpholinothieno[3,2-d]pyrimidine 4 (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 2-chloro-6-iodo-4-morpholinothieno[3,2-d]pyrimidine 19 (3.4 g, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383620B2
Source datasetuspto-grants-2013_02
ORD IDord-5d5b246591d84a47aea4b28f68ffb55a
Source noteuspto-grants-2013_02