Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469863Generated: October 30, 2026

Acetic Acid → HCID 11148749, compound

https://huagongshe.com/reaction/469863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-Amino-5-bromopyrazineHCID 599539—
Reactant3-Cyclopentyloxy-4-methoxybenzaldehydeHCID 2735893—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 11148749HCID 1114874961%

Reaction Steps

A mixture of 3-cyclopentyloxy-4-methoxy-benzaldehyde (417 mg, 1.895 mmol), 2-amino-5-bromopyrazine (300 mg, 1.724 mmol), sodium triacetoxyborohydride (1.5 eq) and glacial acetic acid (3 eq) in dichloromethane (10 ml) was stirred at room temperature overnight. Then the reaction mixture was diluted with ethyl acetate, and washed with water. The oraganic layer was dried over MgSO4 and filtered. The filtrate was concentrated to give the crude product, which was purified by ISCO (SiO2 flash column chromatography) (Hexane/ethyl acetate=100/0 to 3/2) to give about 400 mg of 6-bromo-pyrazin-2-yl)-(3-cyclopentyloxy-4-methoxy-benzyl)-amine. Yield: 61%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629156B2
Source datasetuspto-grants-2014_01
ORD IDord-fc7d0dcfa7ed41449537ca1d45f3bcc4
Source noteuspto-grants-2014_01