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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870286Generated: November 2, 2026

Water → HCID 57404565, compound

https://huagongshe.com/reaction/870286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-MethylimidazoleHCID 1390—
ReactantDifluoromethanesulphonyl chlorideHCID 73932—
Reactant7-fluoro-3-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-1,3-dihydro-2H-indol-2-oneHCID 86706734—
SolventDichloromethaneHCID 6344—
ProductHCID 57404565HCID 57404565—

Reaction Conditions

Temperature0 °C

Reaction Steps

7-Fluoro-3-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-1,3-dihydro-2H-indol-2-one (1.20 g) and 1-methyl-1H-imidazole (0.97 g) are introduced as initial charge in 10 ml of dichloromethane and cooled to 0° C. under nitrogen. With stirring, difluoromethanesulfonyl chloride (1.21 g) is added in 2 portions and the mixture is warmed to room temperature. After 5 hours, 1-methyl-1H-imidazole (0.32 g) and difluoromethanesulfonyl chloride (0.61 g) are added and the mixture is stirred for 16 hours. After adding water and some hydrochloric acid, the solid is filtered off, washed with dichloromethane and water and dried. This gives the title compound as a solid in an HPLC purity of 91% (1.54 g, 92% of theory). The UV absorption (maximum at 360 nm) verifies the N-sulfonylation of the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969553B2
Source datasetuspto-grants-2015_03
ORD IDord-be3e47d2f4dc4fa6ab98093614bbef3b
Source noteuspto-grants-2015_03