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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233981Generated: October 31, 2026

Methanesulfonyl chloride → HCID 86608328, compound

https://huagongshe.com/reaction/2233981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 86608329HCID 86608329—
SolventDimethylformamideHCID 6228—
ProductHCID 86608328HCID 8660832830.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

Methane sulfonyl chloride (0.032 ml, 0.412 mmol) was added dropwise to a solution of 2-(2-aminoethoxy)-6-(4-{[(3,4-dichloro-5-methyl-1H-pyrrol-2-yl)carbonyl]amino}piperidin-1-yl)-N-methoxypyrimidine-4-carboxamide (Example 319, 0.20 g, 0.412 mmol), TEA (0.11 ml, 0.824 mmol) and DMF (3 ml) at 0° C. The reaction was stirred for 15 minutes at 0° C. then quenched with water. The aqueous phase was extracted with EtOAc, washed with saturated sodium bicarbonate solution, water and brine. It was dried over magnesium sulfate and concentrated to give brown solid, which was purified by reverse phase HPLC (30% to 35% acetonitrile in water, 0.1% TFA) affording the title compound (70 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709503B2
Source datasetuspto-grants-2010_05
ORD IDord-54dc5dacab23492487734cd377416ef9
Source noteuspto-grants-2010_05