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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246831Generated: October 26, 2026

Triethylamine → N-carbomethoxy-N'-benzylsulfamoyl-O-methylisourea

https://huagongshe.com/reaction/246831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzylsulfamyl chlorideHCID 13529095—
ReactantMethyl N-(iminomethoxymethyl)carbamateHCID 137319931—
SolventTetrahydrofuranHCID 8028—
ProductN-carbomethoxy-N'-benzylsulfamoyl-O-methylisoureaHCID 70392213—

Reaction Steps

A solution of benzylsulfamoyl chloride (168 g) in anhydrous THF (300 ml) is added dropwise to a stirred solution of N-carbomethoxy-O-methylisourea (107 g) and triethylamine (90 g) in anhydrous THF (800 ml) under nitrogen at -70° C. The resulting suspension is warmed to RT, filtered and the filtrate evaporated in vacuo. The residue is partitioned between methylene chloride and 0.5N aq. HCl. The organic layer is dried, filtered, and concentrated in vacuo affording the desired product as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04704388
Source datasetuspto-grants-1987_11
ORD IDord-4099f6da5a8147cea0efd2977b40bde9
Source noteuspto-grants-1987_11