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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164725Generated: November 3, 2026

Ammonia → 2-(Aminosulfonyl)-N-methoxybenzenecarboximidoyl chloride

https://huagongshe.com/reaction/1164725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant2-(Chlorosulfonyl)-N-methoxybenzenecarboximidoyl chlorideHCID 53742190—
SolventTetrahydrofuranHCID 8028—
Product2-(Aminosulfonyl)-N-methoxybenzenecarboximidoyl chlorideHCID 54018765—

Reaction Conditions

Temperature-30 °C

Reaction Steps

To a solution of the oil prepared in Example 3 in 100 ml of tetrahydrofuran, cooled at -30° C. with external cooling, was added dropwise 1.7 ml of ammonia. After stirring at -30° C. for about 15 minutes, the suspension was purged with N2 to remove excess ammonia, then evaporated at less than 30° C. under vacuum. After adding ice-water to the residue, the suspension was extracted with methylene chloride, dried (MgSO4) and evaporated under vacuum. The residue was triturated with hexane to yield 2.5 g of the subject compound as a crude solid, m.p. 155° to 158° C., NMR(CDCl3 +DMSO):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04906282
Source datasetuspto-grants-1990_03
ORD IDord-20eb8f2542af4f6a84e953a65a25d441
Source noteuspto-grants-1990_03