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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503573Generated: October 30, 2026

(+-)-2-Butanol → N-(5-(7-Methoxyquinolin-4-ylamino)pyrimidin-2-yl)benzamide

https://huagongshe.com/reaction/503573

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+-)-2-ButanolHCID 6568—
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
ReactantSodium BicarbonateHCID 516892—
ReactantN-(5-aminopyrimidin-2-yl)benzamideHCID 11499482—
Reactant8-Chloro-3-methoxy-1,5-naphthyridineHCID 59427340—
SolventDichloromethaneHCID 6344—
ProductN-(5-(7-Methoxyquinolin-4-ylamino)pyrimidin-2-yl)benzamideHCID 67316087—

Reaction Conditions

Temperature100 °C

Reaction Steps

In a screw cap test tube were dissolved 8-chloro-3-methoxy-1,5-naphthyridine (281 mg, 1443 mmol), N-(5-aminopyrimidin-2-yl)benzamide (281 mg, 1312 μmol) and pyridinium p-toluenesulfonate (494 mg, 1968 mmol) in butan-2-ol (2623 μl, 1312 μmol) then heated at 100° C. The reaction turned black in a minute. After 1 h, the reaction mixture showed full conversion to product according to LCMS. The reaction mixture was diluted with CH2Cl2, neutralized with sat. NaHCO3. An emulsion was formed but the two layers eventually separated. The aqueous phase was extracted 3 times with CH2Cl2, washed with brine, dried over MgSO4, filtered and evaporated under reduce pressure to give a tan solid. The solid was triturated with hexane, filtered, and dried under vacuo. Brown solid was collected. LCMS confirmed the presence of the product, N-(5-(7-methoxy-1,5-naphthyridin-4-ylamino)pyrimidin-2-yl)benzamide. MS Calcd for C20H16N6O2: [M]+=372. Found: [M+H]+=373.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776857B2
Source datasetuspto-grants-2010_08
ORD IDord-20a9a2c0f0da489c8456f20c8c800290
Source noteuspto-grants-2010_08