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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170133Generated: October 31, 2026

Methanesulfonyl chloride → (5-Chloromethyl-quinolin-2-yl)-(5-methyl-furan-2-ylmethyl)-amine

https://huagongshe.com/reaction/1170133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactant{2-[(5-Methyl-furan-2-ylmethyl)-amino]-quinolin-5-yl}-methanolHCID 44218152—
SolventTetrahydrofuranHCID 8028—
Product(5-Chloromethyl-quinolin-2-yl)-(5-methyl-furan-2-ylmethyl)-amineHCID 68436366—

Reaction Steps

{2-[(5-Methyl-furan-2-ylmethyl)-amino]-quinolin-5-yl}-methanol (example 41, step A, 70 mg, 0.261 mmol) was dissolved in 2 mL tetrahydrofurane and methanesulfonyl chloride (34 mg, 0.297 mmol) and N,N-diisopropyl ethyl amine (41 mg, 0.318 mmol) were added. The reaction mixture was stirred at room temperature overnight and the solvent was evaporated off. The residue was purified by flash chromatography on silica gel (cyclohexane/ethyl acetate 100:0->50:50 gradient). (5-Chloromethyl-quinolin-2-yl)-(5-methyl-furan-2-ylmethyl)-amine was obtained as a brown solid (59 mg, 79%), MS: m/e=287.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825253B2
Source datasetuspto-grants-2010_11
ORD IDord-e2cac7a370c34b74b95a55a09558e1dd
Source noteuspto-grants-2010_11