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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213415Generated: November 3, 2026

1-(p-Chlorophenyl)cyclobutanecarboxylic acid → HCID 21957244, compound

https://huagongshe.com/reaction/2213415

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(p-Chlorophenyl)cyclobutanecarboxylic acidHCID 602761—
ReactantN-{3-[1-(3-aminopropyl)-4-piperidinyl]phenyl}2-methylpropanamideHCID 16757470—
SolventChloroformHCID 6212—
ProductHCID 21957244HCID 21957244—

Reaction Steps

Example 43 was prepared from 1-(4-chlorophenyl)cyclobutanecarboxylic acid and N-{3-[1-(3-aminopropyl)-4-piperidinyl]phenyl}-2-methylpropanamide according to the procedures described in Scheme 9: 1H NMR (400 MHz, CDCl3) δ 7.56 (s, 1H), 7.41 (s, 1H), 7.34–7.21 (m, 6H), 6.93 (s, 1H), 6.48 (s, 1H), 3.31–3.24 (m, 2H), 2.94–2.86 (m, 2H), 2.86–2.76 (m, 2H), 2.57–2.37 (m, 4H), 2.33–2.26 (m, 2H), 2.12–2.02 (m, 1H), 1.97–1.87 (m, 3H), 1.82 (s, 1H), 1.79 (s, 1H), 1.70–1.56 (m, 4H), 1.24 (d, 6H, J=7.2 Hz); ESMS m/e: 496.3 (M+H)+; Anal. Calc. for C29H38ClN3O2.0.550 CHCl3: C, 63.18; H, 6.92; N, 7.48. Found: C, 63.22; H, 6.90; N, 7.48.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105544B2
Source datasetuspto-grants-2006_09
ORD IDord-b0659f9fc8e843bb8160d20f23e5657d
Source noteuspto-grants-2006_09