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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381066Generated: November 2, 2026

p-Toluenesulfonic acid → HCID 24851913, compound

https://huagongshe.com/reaction/2381066

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHCID 66781834HCID 66781834—
SolventMethanolHCID 887—
ProductHCID 24851913HCID 24851913—

Reaction Steps

p-Toluenesulfonic acid (172 mg, 1.0 mmol) was added to a solution of 8-(cyclopentyloxy)-4-(3,5-dichloropyridin-4-ylamino)-7-methoxy-1-(2-(tetrahydro-2H-pyran-2-yloxy)ethyl)quinolin-2(1H)-one (2.4 g, 4.4 mmol) and methanol (100 mL). After stirring overnight, the reaction was concentrated, diluted with dichloromethane (100 mL), and then washed with sat'd NaHCO3 (20 mL) followed by water (20 mL). The organic layer was dried, filtered, concentrated, and recrystallized from dichloromethane/petroleum ether (1:2) to give 8-(cyclopentyloxy)-4-(3,5-dichloropyridin-4-ylamino)-1-(2-hydroxyethyl)-7-methoxyquinolin-2(1H)-one: 1H NMR (400 MHz, DMSO-d6): δ 8.74 (s, 2H), 8.73 (s, 1H), 7.91 (d, 1H), 7.11 (d, 1H), 4.92 (s, 1H), 4.65 (t, 2H), 4.59 (m, 1H), 4.50 (t, 1H), 3.90 (s, 3H), 3.32 (m 2H), 1.80-1.48 (m, 8H); MS (ESI): 463.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258154B2
Source datasetuspto-grants-2012_09
ORD IDord-24787fcc025149928da61f6c4a837921
Source noteuspto-grants-2012_09