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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401115Generated: October 30, 2026

Acetic Acid → 4-[2-(5-Bromo-pyridin-2-ylamino)-ethyl]-tetrahydro-pyran-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/2401115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1,1-DichloroethaneHCID 6365—
Reactant2-Amino-5-bromopyridineHCID 70622—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactantmethyl 4-(2-oxoethyl)tetrahydro-2H-pyran-4-carboxylateHCID 58468045—
SolventDichloromethaneHCID 6344—
Product4-[2-(5-Bromo-pyridin-2-ylamino)-ethyl]-tetrahydro-pyran-4-carboxylic acid methyl esterHCID 67478678—

Reaction Steps

To a solution of 5-bromopyridin-2-amine (0.488 g, 2.82 mmol) in 1-2 dichloroethane (DCE, 10 mL) was added desired 4-(2-oxo-ethyl)-tetrahydro-pyran-4-carboxylic acid methyl ester (0.529 g, 2.82), acetic acid (3.1 eq) and allowed to stir at room temperature for an hour. NaBH(OAc)3 (3 eq) was then added in one portion and reaction mixture allowed to stir at room temperature for 16 hours. The reaction mixture was then diluted with DCM (10 mL), quenched with 2 M of NH4OH in water. The aqueous layer was extracted with DCM (10 mL×2). The combined organic layers were washed with aqueous NaHCO3 (30 mL), brine (30 mL), and dried over Na2SO4, and concentrated under vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796278B2
Source datasetuspto-grants-2014_08
ORD IDord-1ce9037896ae4782af7e7b40aefd4a15
Source noteuspto-grants-2014_08