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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1349530Generated: October 30, 2026

Acetic Acid → HCID 86592014, compound

https://huagongshe.com/reaction/1349530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-EthylbutyraldehydeHCID 7359—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 86592010HCID 86592010—
SolventDichloromethaneHCID 6344—
ProductHCID 86592014HCID 8659201483%

Reaction Steps

(±)-Cis-N-{1-[4-(2-ethyl-butylamino)-benzoyl]-2-methyl-1,2,3,4-tetrahydro-quinolin-4-yl}-N-phenyl-propionamide was prepared from (±)-cis-N-[1-(4-amino-benzoyl)-2-methyl-1,2,3,4-tetrahydro-quinolin-4-yl]-N-phenyl-propionamide. To a solution of (±)-cis-N-[1-(4-Amino-benzoyl)-2-methyl-1,2,3,4-tetrahydro-quinolin-4-yl]-N-phenyl-propionamide (75 mg, 0.145 mmol) in dichloromethane (3 mL) was added 2-ethylbutyraldehyde (26 uL, 0.2 mmol) in one portion. The mixture was stirred at room temperature for a 0.5 h before a solution of sodium triacetoxyborohydride (74 mg, 0.348 mmol) 1 ml DCM was added slowly. A single drop of acetic acid was added and the reaction was allowed to stir at room temperature over night. Excess reagent was quenched by the addition of saturated aqueous sodium bicarbonate. The resulting mixture was extracted three times with 20 mL dichloromethane. The combined extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated. Crude product was purified by HPLC to afford the title compound (60 mg, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07211672B2
Source datasetuspto-grants-2007_05
ORD IDord-7eab92a2c37d4aa8955fc696a4c923d1
Source noteuspto-grants-2007_05