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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181229Generated: October 25, 2026

Diisopropylethylamine → Benzyl sulfamic acid-[6-chloro-5-(p-chloro-phenyl)-4-pyrimidinyl]-amide

https://huagongshe.com/reaction/1181229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4,6-Dichloro-5-(4-chlorophenyl)-pyrimidineHCID 21979569—
ReactantBenzylsulfamic acid amide potassium saltHCID 68727905—
SolventDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
ProductBenzyl sulfamic acid-[6-chloro-5-(p-chloro-phenyl)-4-pyrimidinyl]-amideHCID 2197954444.1%

Reaction Steps

To 4,6-dichloro-5-(4-chloro-phenyl)-pyrimidine (Referential Example 9) (2.59 g) dissolved in DMSO (14 ml) was added di-isopropyl-ethyl-amine (1.8 ml) followed by the addition of benzyl sulfamic acid amide potassium salt (2.25 g) [prepared from the product described in Referential Example 22 and potassium tert.-butylate in methanol followed by the evaporation of the solvent]. The mixture was stirred for 24 h at rt then poured onto water (300 ml) and diethylether (120 ml) was added and the solution was stirred for 30 min. The layers were separated and the water layer was acidified with solid citric acid (pH=3) and cooled to 0° C. for 1 h. The precipitated product was filtered off, washed with water and recrystallized from methanol to give benzyl sulfamic acid-[6-chloro-5-(p-chloro-phenyl)-4-pyrimidinyl]-amide (1.8 g). tR=4.94 min (LC); [M+H]+=410.90 (ES+);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285549B2
Source datasetuspto-grants-2007_10
ORD IDord-f82d3ea703c14a34a341b60e9fe024f9
Source noteuspto-grants-2007_10