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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894303Generated: November 3, 2026

Methanesulfonyl chloride → HCID 58049436, compound

https://huagongshe.com/reaction/1894303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzyl (1-(hydroxymethyl)cyclopropyl)carbamateHCID 22178711—
SolventDichloromethaneHCID 6344—
ProductHCID 58049436HCID 58049436—

Reaction Conditions

Temperature0 °C

Reaction Steps

N—CBZ-amino-1-(hydroxymethyl)cyclopropane (similarly prepared according to JMC 31, 2004, 1998) (250 mg) was dissolved into DCM (25 ml) with DIPEA (250 l) and stirred at 0° C. for 15 minutes. To the reaction was added MsCl (1.1 eq) and stirred for 30 minutes. The reaction was washed with NaHCO3 solution, water, brine and dried with Na2SO4. The solution was evaporated to give N—CBZ-amino-1-(methylsulfonyloxymethyl)cyclopropane as an off white solid. This solid was mixed with above 6-(7-hydroxy-6-methoxyquinolin-4-yloxy)-N-methyl-1-naphthamide and Cs2CO3 (250 mg) in DMA (4 ml). The reaction was heated at 100° C. for 10 hours and mixed with EtOAc and water, then filtered, further extracted with EtOAc. The combined organic layer was evaporated and purified with silica gel column to give the titled product. Mass: (M+1), 578

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513283B2
Source datasetuspto-grants-2013_08
ORD IDord-0b9f8b587bd84702a1dab5a101ce1dda
Source noteuspto-grants-2013_08