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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522813Generated: October 29, 2026

p-Toluenesulfonic acid → HCID 24851913, compound

https://huagongshe.com/reaction/1522813

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 stifling 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 numberUS09078887B2
Source datasetuspto-grants-2015_07
ORD IDord-59808fee21974c63a2e7b4dbdd64d961
Source noteuspto-grants-2015_07