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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365131Generated: November 1, 2026

Iodine → 2-Chloro-6-iodo-4-morpholinofuro[3,2-d]pyrimidine

https://huagongshe.com/reaction/1365131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant2-Chloro-4-morpholinofuro[3,2-d]pyrimidineHCID 56833741—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-Chloro-6-iodo-4-morpholinofuro[3,2-d]pyrimidineHCID 5959307083%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 2-chloro-4-morpholinofuro[3,2-d]pyrimidine 38 (50 mg, 1.0 eq) dissolved in THF (2.1 ml) at −78° C. was added 1.6M solution of n-butyllithium (0.17 ml, 1.3 eq, 1.6M in hexanes). Reaction mixture was stirred at −78° C. for 30 minutes. A solution of iodine (159 mg, 3.0 eq) in THF (0.6 ml) was added and reaction mixture was allowed to slowly warm up to room temperature and stirred for 45 minutes. The reaction mixture was quenched with saturated aq. Na2S2O3, and extracted with dichloromethane. The combined organic layers were dried (Na2SO4) and concentrated. The crude reaction mixture was purified by flash chromatography to yield 2-chloro-6-iodo-4-morpholinofuro[3,2-d]pyrimidine 45 (63 mg, 83%): MS (Q1) 366 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888352B2
Source datasetuspto-grants-2011_02
ORD IDord-d3f7016e36264369854119bcad4e62e9
Source noteuspto-grants-2011_02