Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269231Generated: October 30, 2026

Bis(4-chlorophenyl)acetic acid → N-{3-[1-(3-{[2,2-bis(4-chlorophenyl)acetyl]amino}propyl)-4-piperidinyl]phenyl}butanamide

https://huagongshe.com/reaction/1269231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBis(4-chlorophenyl)acetic acidHCID 6730—
ReactantN-{3-[1-(3-aminopropyl)-4-piperidinyl]phenyl}butanamideHCID 21957120—
ProductN-{3-[1-(3-{[2,2-bis(4-chlorophenyl)acetyl]amino}propyl)-4-piperidinyl]phenyl}butanamideHCID 21957203—

Reaction Steps

Example 53 was prepared from bis(4-chlorophenyl)acetic acid and N-{3-[1-(3-aminopropyl)-4-piperidinyl]phenyl}butanamide according to the procedures described in Scheme 10: 1H NMR (400 MHz, CDCl3) δ 7.67 (s, 1H), 7.58 (s, 1H), 7.49 (br s, 1H), 7.28–7.21 (m, 10H), 6.91 (m, 1H), 4.77 (s, 1H), 3.38 (dd, 2H, J=6.0, 11.6 Hz), 2.93 (d, 2H, J=11.6 Hz), 2.46 (m, 1H), 2.41 (t, 2H, J=6.0 Hz), 2.31 (t, 2H, J=7.2 Hz), 1.96 (dt, 2H, J=1.6, 12.0 Hz); 1.82–1.66 (m, 6H), 1.58–1.54 (m, 2H), 0.98 (t, 3H, J=7.6 Hz); ESMS m/e: 566.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199135B2
Source datasetuspto-grants-2007_04
ORD IDord-d8cc724dbe7244938756b066444bbe0e
Source noteuspto-grants-2007_04