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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2087205Generated: October 30, 2026

Propionyl chloride → 2-methyl-N-(3-{1-[(3S)-3-phenyl-3-(propionylamino)propyl]-4-piperidinyl}phenyl)propanamide

https://huagongshe.com/reaction/2087205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropionyl chlorideHCID 62324—
ReactantN-(3-{1-[(3S)-3-(acetylamino)-3-phenylpropyl]-4-piperidinyl)phenyl)-2-methylpropanamideHCID 69523292—
ReactantN-(3-(1-[(3S)-3-amino-3-phenylpropyl]-4-piperidinyl)phenyl)-2-methylpropanamideHCID 69523474—
Product2-methyl-N-(3-{1-[(3S)-3-phenyl-3-(propionylamino)propyl]-4-piperidinyl}phenyl)propanamideHCID 2072297697%

Reaction Steps

According to the procedure used for the synthesis of N-(3-{1-[(3S)-3-(acetylamino)-3-phenylpropyl]-4-piperidinyl}phenyl)-2-methylpropanamide, N-(3-{1-[(3S)-3-amino-3-phenylpropyl]-4-piperidinyl}phenyl)-2-methylpropanamide (11.0 mg, 0.0280 mmol) and propionyl chloride (3.80 mg, 0.0420 mmol) provided 2-methyl-N-(3-{1-[(3S)-3-phenyl-3-(propionylamino)propyl]-4-piperidinyl}phenyl)propanamide (12 mg, 97% yield). 1H NMR (400 MHz, CDCl3) δ 8.05 (s, 1H), 7.59 (s, 1H), 7.40-7.20 (m, 7H), 6.96 (s, 1H), 5.19-5.12 (m, 1H), 3.18 (d, 1H, J=12.0 Hz), 2.99 (d, 1H, J=10.4 Hz), 2.93-2.86 (m, 1H), 2.61-2.40 (m, 3H), 2.38-2.23 (m, 3H), 2.19-1.75 (m, 8H), 1.25 (d, 6H, J=6.9 Hz), 1.22-1.08 (m, 3H); ESMS m/e: 436.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06727264B1
Source datasetuspto-grants-2004_04
ORD IDord-fa9743a797084461b1b97f21cf75a76c
Source noteuspto-grants-2004_04