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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032547Generated: October 26, 2026

Ethylmorpholine → N-(4-cyanomethyl-1H-indazol-7-yl)methanesulfonamide

https://huagongshe.com/reaction/1032547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylmorpholineHCID 7525—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-(7-amino-1H-indazol-4-yl)acetonitrileHCID 19354434—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-cyanomethyl-1H-indazol-7-yl)methanesulfonamideHCID 22166017—

Reaction Steps

At 0° C., 1.7 g of 2-(7-amino-1H-indazol-4-yl)acetonitrile in 15 ml of dimethylformamide and 5 ml of tetrahydrofuran is combined with 0.96 ml of methanesulfonyl chloride and 1.56 ml of N-ethylmorpholine and agitated for 16 hours at room temperature. The mixture is concentrated, chromatographed over silica gel with methanol/dichloromethane (1:3), and recrystallized from methanol, thus producing 2.2 g of N-(4-cyanomethyl-1H-indazol-7-yl)methanesulfonamide, mp 223°-225° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04958026
Source datasetuspto-grants-1990_09
ORD IDord-d554e39a32904f1b8574b3b62861c667
Source noteuspto-grants-1990_09