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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064315Generated: November 2, 2026

Diethylmethylamine → HCID 22273523, compound

https://huagongshe.com/reaction/1064315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylmethylamineHCID 12022—
ReactantThionyl ChlorideHCID 24386—
ReactantChlorosulfonic acidHCID 24638—
Reactant4-Amino-1-butanolHCID 25868—
ReactantHCID 22273557HCID 22273557—
SolventMethanolHCID 887—
ProductHCID 22273523HCID 2227352379%

Reaction Conditions

Temperature0 °C

Reaction Steps

Chlorosulphonic acid (150 μl, 2.16 mmol) was added dropwise to a solution of 2-anilino-4-(1-ethyl-2-methylimidazol-5-yl)pyrimidine (Example 28; 150 mg, 0.54 mmol) in thionyl chloride (3 ml) cooled to 0° C. and the mixture stirred for 10 minutes at 0° C. then heated at 90° C. for 90 minutes. The volatiles were removed by evaporation and the resultant solid placed under high vacuum (<2 mmHg) for 1 hr. The resulting solid was placed under nitrogen and a solution of 2-(2-aminoethyl)ethanol (114 mg, 1.00 mmol) and diethylmethylamine in MeOH (3 ml) was cautiously added. The solution was stirred for 30 minutes and the volatiles were evaporated. Water (20 ml) was added and the precipitated solid was collected by filtration and washed with water (2×10 ml). The residue was dissolved in MeOH (5 ml) and loaded on to an Isolute amine column, eluted with MeOH (30 ml) and the fractions containing product were evaporated to give the title compound (190 mg, 79%) as a beige solid. NMR 1.18 (t, 3H), 2.39 (s, 3H), 2.89 (t, 2H), 3.15 (m, 7H), 4.38 (q, 2H), 7.21 (d, 1H), 7.71 (m, 3H), 7.89 (d, 2H), 8.41 (d, 1H), 9.82 (s, 1H); m/z 447.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969714B2
Source datasetuspto-grants-2005_11
ORD IDord-e8bfac32f8564dd0aaaf6c8950cb0a15
Source noteuspto-grants-2005_11