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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966526Generated: November 1, 2026

2-Mercaptobenzoic Acid → N-(2-{2-Methyl-4-[((S)-phenyl-(S)-piperidin-2-yl-methyl)-amino]-quinolin-8-yloxy}-ethyl)methanesulfonamide dihydrochloride

https://huagongshe.com/reaction/1966526

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Mercaptobenzoic AcidHCID 5443—
ReactantSodium HydroxideHCID 14798—
Reactant1,4-Bis(diphenylphosphino)butaneHCID 82124—
ReactantIsopropanol-hcl-waterHCID 21409480—
ReactantN-[2-(4-{[(S)-((S)-1-Allylpiperidin-2-yl)-phenylmethyl]-amino}-2-methylquinolin-8-yloxy)ethyl]methanesulfonamideHCID 59474734—
SolventTetrahydrofuranHCID 8028—
ProductN-(2-{2-Methyl-4-[((S)-phenyl-(S)-piperidin-2-yl-methyl)-amino]-quinolin-8-yloxy}-ethyl)methanesulfonamide dihydrochlorideHCID 6849858230%

Reaction Steps

Tris-(dibenzylidenaceton)-dipalladium(0) (19.0 mg, 0.021 mmole) and 1,4-bis(diphenylphosphino)butane (9 mg, 0.021 mmole) were mixed with THF (10 mL). N-[2-(4-{[(S)—((S)-1-Allylpiperidin-2-yl)-phenylmethyl]-amino}-2-methylquinolin-8-yloxy)-ethyl]-methanesulfonamide (example 35, 130 mg, 0.256 mmole) in THF (5 mL) and 2-mercaptobenzoic acid (86.7 mg, 0.562 mmole) in THF (5 mL) were added and the mixture was stirred at RT for 2 hrs. The content of the flask was mixed with 1N NaOH and extracted with dichloromethane. The organic layer was washed with water and saturated NaCl solution and concentrated. The residue thus obtained was cystallized from isopropanol/water/HCl to obtain a white solid (42 mg, 30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420670B2
Source datasetuspto-grants-2013_04
ORD IDord-69cc82f3695b4a3b8d63c256525f999d
Source noteuspto-grants-2013_04