Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755938Generated: November 2, 2026

Water → N-[1-[(3-Methoxyphenyl)methyl]-4-piperidinyl]-8-methoxy-4-[[4-[[[1-(phenylmethyl)-4-piperidinyl]amino]carbonyl]phenyl]amino]-3-quinoline-carboxamide

https://huagongshe.com/reaction/1755938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,4-Dioxa-8-azaspiro(4.5)decaneHCID 67435—
Reactant3-Methoxybenzyl chlorideHCID 69994—
Reactant1-[(3-Methoxyphenyl)methyl]piperidin-4-amineHCID 12641840—
Reactant8-Methoxy-4-[[4-[[[1-(phenylmethyl)-4-piperidinyl]amino]carbonyl]phenyl]amino]-3-quinolinecarboxylic acidHCID 15289772—
ProductN-[1-[(3-Methoxyphenyl)methyl]-4-piperidinyl]-8-methoxy-4-[[4-[[[1-(phenylmethyl)-4-piperidinyl]amino]carbonyl]phenyl]amino]-3-quinoline-carboxamideHCID 19918426—

Reaction Steps

N-[1-[(3-Methoxyphenyl)methyl]-4-piperidinyl]-8-methoxy-4-[[4-[[[1-(phenylmethyl)-4-piperidinyl]amino]carbonyl]phenyl]amino]-3-quinoline-carboxamide was prepared as a hygroscopic solid (0.76 hydrate) by coupling 8-methoxy-4 -[[4-[[[1-(phenylmethyl)-4-piperidinyl]amino]carbonyl]phenyl]amino]-3-quinolinecarboxylic acid and 1-[(3-methoxyphenyl)methyl]-4-piperidinamine as described for Example 17, Step 5. 1-[(3-Methoxyphenyl)methyl]-4-piperidinamine can be prepared from 3-methoxybenzyl chloride and 1,4-dioxa-8-azaspiro[4.5]-decane as described in U.S. Pat. Nos. 3,875,165 and 4,816,464: mp 135°-142° C.; 1H NMR (Me2SO-d6, 400 MHz) δ 9.48 (s, 1 H), 8.76 (s, 1 H), 8.39 (d, J=7.5 Hz, 1 H), 7.98 (d, J=7.7 Hz, 1 H), 7.68 (d, J=8.6 Hz, 2 H), 7.57 (d, J=8.6 Hz, 1H), 7.41 (m, 1H), 7.10-7.35 (m, 8 H), 6.7-6.9 (m, 4 H), 3.94 (s, 3 H), 3.6-3.8 (m, 4 H), 3.2-3.6 (m, 5 H), 2.6-2.9 (m, 4 H), 1.3-2.1 (m, 12 H); Karl Fischer, 0.76 moles of H2O.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05438064
Source datasetuspto-grants-1995_08
ORD IDord-d1b183bd33cd458b8f4222466dd0413d
Source noteuspto-grants-1995_08