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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127137Generated: October 30, 2026

5-(N,N-Dimethylaminosulfonyl)-1,3,4-thiadiazol-2-yl isocyanate → N-[5-(N,N-dimethylaminosulfonyl)-1,3,4-thiadiazol-2-yl]-N'-[2,2-dimethyl-2-(4-methyl-1,3-dioxan-2-yl)ethyl]-N'-methylurea

https://huagongshe.com/reaction/127137

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(N,N-Dimethylaminosulfonyl)-1,3,4-thiadiazol-2-yl isocyanateHCID 12894454—
ReactantN-[2,2-dimethyl-2-(4-methyl-1,3-dioxan-2-yl)ethyl]methylamineHCID 12894460—
SolventEthyl AcetateHCID 8857—
ProductN-[5-(N,N-dimethylaminosulfonyl)-1,3,4-thiadiazol-2-yl]-N'-[2,2-dimethyl-2-(4-methyl-1,3-dioxan-2-yl)ethyl]-N'-methylureaHCID 20286115—

Reaction Steps

5-(N,N-Dimethylaminosulfonyl)-1,3,4-thiadiazol-2-yl isocyanate dimer (6 grams) N-[2,2-dimethyl-2-(4-methyl-1,3-dioxan-2-yl)ethyl]methylamine (6 grams) and ethyl acetate (20 ml) are charged into a glass reaction vessel fitted with a mechanical stirrer. The reaction mixture is heated on a steam bath for a period of about 2 hours. Solvent is then stripped off using a rotary evaporator to yield the desired product N-[5-(N,N-dimethylaminosulfonyl)-1,3,4-thiadiazol-2-yl]-N-[2,2-dimethyl-2-(4-methyl-1,3-dioxan-2-yl)ethyl]-N-methylurea as the residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04255182
Source datasetuspto-grants-1981_03
ORD IDord-ca83e0dc9c624a6c84dae401a1a4125e
Source noteuspto-grants-1981_03