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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732191Generated: October 30, 2026

Propanal → Methyl 3-[4-({3-[[(4-phenyl-1,3-thiazol-2-yl)methyl](propyl)amino]benzyl}oxy)phenyl]propanoate

https://huagongshe.com/reaction/732191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropanalHCID 527—
Reactant4-Phenyl-1,3-thiazole-2-carbaldehydeHCID 3538814—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantMethyl 3-{4-[(3-aminobenzyl)oxy]phenyl}-propanoateHCID 23143302—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductMethyl 3-[4-({3-[[(4-phenyl-1,3-thiazol-2-yl)methyl](propyl)amino]benzyl}oxy)phenyl]propanoateHCID 2314325478.5%

Reaction Steps

To a mixture of 4-phenyl-1,3-thiazole-2-carbaldehyde (210 mg, 1.1 mmol), methyl 3-{4-[(3-aminobenzyl)oxy]phenyl}-propanoate (285 mg, 1.0 mmol), acetic acid (0.2 mL) and 1,2-dichloroethane (5 mL) was added sodium triacetoxyborohydride (0.6 g, 2.8 mmol) under ice-cooling, and the mixture was warmed to room temperature and stirred for 1 hr. Propanal (200 mg, 3.4 mmol) was added to the reaction mixture, and the mixture was further stirred at room temperature for 1 hr. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:19-1:2 in volume ratio) to give the title compound (393 mg, yield 78%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585880B2
Source datasetuspto-grants-2009_09
ORD IDord-fcf9313ff1bb41baac2c41f165c80b30
Source noteuspto-grants-2009_09