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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881330Generated: November 1, 2026

Acetic Acid → N-((2-chloro-7-methyl-4-morpholinothieno[3,2-d]pyrimidin-6-yl)methyl)-N,1-dimethylpiperidin-4-amine

https://huagongshe.com/reaction/881330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1-Methyl-4-(methylamino)piperidineHCID 566323—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-Chloro-7-methyl-4-morpholinothieno[3,2-d]pyrimidine-6-carbaldehydeHCID 56648582—
Solvent1,2-DichloroethaneHCID 11—
SolventSodium BicarbonateHCID 516892—
ProductN-((2-chloro-7-methyl-4-morpholinothieno[3,2-d]pyrimidin-6-yl)methyl)-N,1-dimethylpiperidin-4-amineHCID 8662352588%

Reaction Steps

2-Chloro-7-methyl-4-morpholinothieno[3,2-d]pyrimidine-6-carbaldehyde (0.5 g) was dissolved in 10 mL of 1,2-DCE and 1.0 eq. AcOH and 1.3 eq. of 1-methyl-4-(methylamino)piperidine was added and the reaction was stirred 15 minutes followed by the addition of sodium triacetoxyborohydride. The reaction was stirred for 24 hours and product formation was confirmed by LCMS. The reaction was diluted with sat. NaHCO3, extracted with dichloromethane, dried over MgSO4 and concentrated in vacuo. The crude product was purified by flash chromatography (EtOAc/hexanes) to give 0.61 g N-((2-chloro-7-methyl-4-morpholinothieno[3,2-d]pyrimidin-6-yl)methyl)-N,1-dimethylpiperidin-4-amine (88% yield). MS (Q1) 411 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993563B2
Source datasetuspto-grants-2015_03
ORD IDord-2e851f76cd6b4d6991aefddbb3fc9bad
Source noteuspto-grants-2015_03