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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098717Generated: October 30, 2026

Sodium hydride → HCID 86618412, compound

https://huagongshe.com/reaction/2098717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantN-(2-methoxyethyl)methanesulfonamideHCID 3522477—
Reactant4-(6-(Bromomethyl)-2-chlorothieno[3,2-d]pyrimidin-4-yl)morpholineHCID 46180726—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86618412HCID 8661841274%

Reaction Steps

To a solution of N-(2-Methoxy-ethyl)-methanesulfonamide (61 mg) in tetrahydrofuran (1.5 ml) under nitrogen was added sodium hydride, 60% dipersion in mineral oil, (18 mg). The reaction mixture was stirred at room temperature for 30 minutes. 6-Bromomethyl-2-chloro-4-morpholin-4-yl-thieno[3,2-d]pyrimidine (140 mg) was added. The reaction mixture was stirred at room temperature for 2 hours and then 50° C. for 5 hours. The solvents were removed in vacuo to give a crude product. This was purified by flash chromatography to give N-(2-Chloro-4-morpholin-4-yl-thieno[3,2-d]pyrimidin-6-ylmethyl)-N-(2-methoxy-ethyl)-methanesulfonamide (124 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450315B2
Source datasetuspto-grants-2013_05
ORD IDord-21cf1d8d27c4414aa3d1dec03bd5bfd3
Source noteuspto-grants-2013_05