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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391095Generated: October 29, 2026

Acetic Acid → 1-((2-Chloro-4-morpholinothieno[2,3-d]pyrimidin-6-yl)methyl)piperidin-4-ol

https://huagongshe.com/reaction/391095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPiperidin-4-olHCID 79341—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-Chloro-4-morpholinothieno[2,3-d]pyrimidine-6-carbaldehydeHCID 56833844—
Solvent1,2-DichloroethaneHCID 11—
Product1-((2-Chloro-4-morpholinothieno[2,3-d]pyrimidin-6-yl)methyl)piperidin-4-olHCID 5823391241.7%

Reaction Steps

To a solution of 2-chloro-4-morpholinothieno[2,3-d]pyrimidine-6-carbaldehyde (1.1 g, 3.9 mmol) in 1,2-dichloroethane (20 mL) was added piperidin-4-ol (5.4 mmol), and AcOH (3.9 mmol). After the reaction mixture stirred 10 min at room temperature, Na(OAc)3BH (4.6 mmol) was added and the mixture stirred 72 h at room temperature. The reaction was quenched by the addition of saturated aqueous NaHCO3. The organic layer was separated and the aqueous layer was extracted with CH2Cl2. The combined organics were dried over Na2SO4 and concentrated in vacuo. The crude reaction was purified by silica gel chromatography (0-20% MeOH in CH2Cl2) to afford 1-((2-chloro-4-morpholinothieno[2,3-d]pyrimidin-6-yl)methyl)piperidin-4-ol (0.6 g). MS (Q1) 369 (M)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383620B2
Source datasetuspto-grants-2013_02
ORD IDord-9c016312db5b4fe6a82d2e6b0756ad7f
Source noteuspto-grants-2013_02