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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888913Generated: October 28, 2026

Sodium borohydride → (2-Chloro-4-morpholinothieno[3,2-d]pyrimidin-6-yl)methanol

https://huagongshe.com/reaction/888913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-Chloro-4-morpholinothieno[3,2-d]pyrimidine-6-carbaldehydeHCID 45789985—
SolventTetrahydrofuranHCID 8028—
Product(2-Chloro-4-morpholinothieno[3,2-d]pyrimidin-6-yl)methanolHCID 4618060591%

Reaction Steps

To a suspension of 2-chloro-4-morpholin-4-yl-thieno[3,2-d]pyrimidine-6-carbaldehyde (3.2 g, 11.31 mmol) in anhydrous THF (100 mL) and IMS (70 mL) was added sodium borohydride (0.47 g, 12.42 mmol) and the resulting mixture stirred at RT for 2 h. The reaction mixture was partitioned between DCM and a sat. aqueous solution of NaHCO3. The organic layer was isolated, dried (MgSO4) and concentrated in vacuo. The resultant residue was triturated with water gave the title compound as a white solid (2.9 g, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08252792B2
Source datasetuspto-grants-2012_08
ORD IDord-be4e02733702487591e08ab405933524
Source noteuspto-grants-2012_08