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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416338Generated: November 1, 2026

Triethylamine → n-[4'-(2,4-Diamino-pyrimidin-5-ylmethyl)-2',6'-diethoxy-biphenyl-3-yl]-methanesulphonamide

https://huagongshe.com/reaction/2416338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant5-(3'-Amino-2,6-diethoxy-biphenyl-4-ylmethyl)-pyrimidine-2,4-diamineHCID 9864620—
SolventDimethylformamideHCID 6228—
Productn-[4'-(2,4-Diamino-pyrimidin-5-ylmethyl)-2',6'-diethoxy-biphenyl-3-yl]-methanesulphonamideHCID 22636769—

Reaction Conditions

Temperature0 °C

Reaction Steps

5-(3′-Amino-2,6-diethoxy-biphenyl-4-ylmethyl)-pyrimidine-2,4-diamine (228 mg; 0.6 mmol) is dissolved in dimethylformamide (6 ml; dried over a molecular sieve), triethylamine (0.090 ml; 0.66 mmol) is added at room temperature, and the mixture is cooled to 0° C. and a solution of methanesulphonyl chloride (0.051 ml; 0.66 mmol) in dimethylformamide (1.0 ml) is added in the course of 5 minutes. After 1 hour at 0-5° C. the reaction mixture is concentrated and the residue is taken up in water, after which the pH is adjusted to 10 by addition of NH4OH conc. After stirring for 15 minutes the mixture is filtered with suction and the residue is dried under a high vacuum and chromatographed over silica gel (60 g) with methylene chloride/methanol/NH4OH conc. (19/1/0.05).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06821980B1
Source datasetuspto-grants-2004_11
ORD IDord-bc344275c5ad4d4dbb7bd28ba6ee2f3f
Source noteuspto-grants-2004_11