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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269298Generated: October 27, 2026

2,2-Diphenylbutyric acid → N-[3-(1-{3-[(2,2-Diphenylbutanoyl)amino]propyl}4-piperidinyl)phenyl]cyclopropanecarboxamide

https://huagongshe.com/reaction/1269298

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-Diphenylbutyric acidHCID 77902—
ReactantN-{3-[1-(3-aminopropyl)4-piperidinyl]phenyl}cyclopropanecarboxamideHCID 21957166—
ProductN-[3-(1-{3-[(2,2-Diphenylbutanoyl)amino]propyl}4-piperidinyl)phenyl]cyclopropanecarboxamideHCID 21957220—

Reaction Steps

Example 122 was prepared from 2,2-diphenylbutanoic acid and N-{3-[1-(3-aminopropyl)-4-piperidinyl]phenyl}cyclopropanecarboxamide according to the procedures described in Scheme 10: 1H NMR (400 MHz, CDCl3) δ 7.89–7.74 (br, 1H), 7.48–7.05 (m, 13H), 6.89–6.74 (d, 1H, J=7.2 Hz), 6.46–6.25 (br, 1H), 3.30–3.15 (m, 2H), 3.15–3.01 (m, 2H), 2.38–2.25 (m, 3H), 2.25–2.09 (m, 2H), 1.99–1.78 (m, 3H), 1.78–1.60 (m, 5H), 1.60–1.47 (m, 1H), 1.12–1.01 (m, 2H), 0.90–0.71 (m, 2H), 0.75 (t, 3H, J=7.2 Hz); ESMS m/e: 524.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199135B2
Source datasetuspto-grants-2007_04
ORD IDord-01de20246dd549e9ba0e0cb2c74ec56d
Source noteuspto-grants-2007_04