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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390870Generated: October 29, 2026

Acetic Acid → HCID 58234055, compound

https://huagongshe.com/reaction/390870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1-(2-Hydroxyethyl)piperazineHCID 7677—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-Aminopyrimidine-5-boronic acid, pinacol esterHCID 17750212—
Reactant2-Chloro-4-morpholinothieno[3,2-d]pyrimidine-6-carbaldehydeHCID 45789985—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 58234055HCID 58234055—

Reaction Steps

To a solution of 2-chloro-4-morpholinothieno[3,2-d]pyrimidine-6-carbaldehyde (1.3 g, 4.6 mmol) in 1,2-dichloroethane (45 mL) was added 1-(2-hydroxyethyl)piperazine (0.8 mL, 6.4 mmol) and AcOH (260 μL, 4.6 mmol). After stirring 10 min at room temperature, Na(OAc)3BH (1.2 g, 5.5 mmol) was added and the resulting mixture stirred overnight. The reaction was quenched by the addition of saturated aqueous NaHCO3 and the organic layer was separated. The aqueous layer was extracted with CH2Cl2 and the combined organics were dried over Na2SO4, filtered, and concentrated in vacuo. A portion (0.4 mmol) of the crude intermediate was coupled following General Procedure A with 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-amine to provide 158 after reverse phase HPLC purification (15 mg). MS (Q1) 457 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383620B2
Source datasetuspto-grants-2013_02
ORD IDord-1af927f1c3eb43d78767dbe4c32c7cd0
Source noteuspto-grants-2013_02