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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245887Generated: November 1, 2026

Potassium Hydroxide → HCID 58815876, compound

https://huagongshe.com/reaction/2245887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant4-Aminobutyrate ethyl hydrochlorideHCID 12649661—
ReactantHCID 58815870HCID 58815870—
SolventEthanolHCID 702—
ProductHCID 58815876HCID 5881587654.4%

Reaction Steps

A 100 mL round bottom flask equipped with a magnetic stir bar was flushed with nitrogen and charged with 2.31 g (5 mmol, 1 eq) of 1-{3-[(R)-((2S,5R)-4-allyl-2,5-dimethyl-1-piperazinyl)(3-hydroxyphenyl)-methyl]-benzoyl}-4-piperidinone (Example 136), 1.41 g (8.4 mmol, 1.68 eq) of ethyl 4-aminobutyrate hydrochloride, 0.47 g (8.4 mmol, 1.68 eq) of potassium hydroxide, and 10 mL of ethanol. The reaction was stirred vigorously at room temperature under nitrogen for 2.5 hours. A solution of 0.32 g (5 mmol, 1 eq) of sodium cyanoborohydride in 5 mL of ethanol was added and the reaction was stirred overnight. The reaction was quenched by careful addition of 1 mL of saturated aqueous NH4Cl solution and stirred vigorously for 30 minutes and concentrated in vacuo. The residue was partitioned between 50 mL dichloromethane and water, and the aqueous solution was adjusted to pH=8-9 using saturated sodium bicarbonate solution. The organic layer was separated and dried over sodium sulfate/magnesium sulfate and the solvent was removed in vacuo, leaving 2.81 g of crude product as a viscous, amber-colored oil. Chromatography of this material on a pre-packed 4×15 cm Biotage® silica gel cartridge eluting with dichloromethane/ethyl acetate with 2% ammonium hydroxide yielded 1.57 g (53%) of 4-(1-{3-[(R)-((2S,5R)-4-Allyl-2,5-dimethyl-piperazin-1-yl)-(3-hydroxy-phenyl)-methyl]-benzoyl}-piperidin-4-ylamino)-butyric acid ethyl ester as an off-white foam. Calculated for C34H48N4O4 0.1 CH2Cl2: %C, 69.98; H, 8.30; N, 9.57. Found: %C, 70.07; H, 8.39; N, 9.65. 1H NMR (300 MHz, CDCl3): {tilde over (□)}{tilde over (□)}1{tilde over (□)}1m, 1H), 7.38-7.23 (m, 3H), 7.11 (t, J=7.9 Hz, 1H), 6.68-6.56 (m, 1H), 6.65 (t, J=7.9 Hz, 2H), 5.93-5.80 (m, 1H), 5.21-5.14 (m, 3H), 4.52 (br s, 1H), 4.14 (q, J=7.2 Hz, 2H), 3.67 (m, 1H), 3.36 (br d, 1H), 2.98-2.78 (m, 4H), 2.73-2.55 (m, 5H), 2.46 (m, 1H), 2.37 (t, J=7.2 Hz, 2H), 2.12 (dd, J=1, 9.3 Hz, 1H), 1.92 (m, 1H), 1.79 (quint, J=7.1 Hz, 2H), 1.26 (t, J=7.1 Hz, 3H), 1.15 (br d, J=5.6 Hz, 3H), 0.98 (d, J=6.2 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683168B2
Source datasetuspto-grants-2010_03
ORD IDord-e92dca3c485a4b02af7ab6a081e495f0
Source noteuspto-grants-2010_03