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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098885Generated: November 1, 2026

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

https://huagongshe.com/reaction/2098885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactantn-Butyl lithiumHCID 61028—
Reactant2-Chloro-4-(morpholin-4-yl)thieno(3,2-d)pyrimidineHCID 20284971—
SolventTetrahydrofuranHCID 8028—
Product4-(2-Chloro-6-iodothieno[3,2-d]pyrimidin-4-yl)morpholineHCID 5959306175.9%

Reaction Conditions

Temperature-40 °C

Reaction Steps

N-Butyllithium (9.4 mL, 22.48 mmol, 2.5 M in hexane solution) was added to a mixture of 2-chloro-4-morpholinothieno[3,2-d]pyrimidine (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 (300 mL) 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 (3.4 g, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450315B2
Source datasetuspto-grants-2013_05
ORD IDord-4e313c46a20b42738cbbfe533d34d2e2
Source noteuspto-grants-2013_05