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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117744Generated: October 30, 2026

Chlorosulfonic acid → HCID 69314314, compound

https://huagongshe.com/reaction/2117744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
ReactantCyclopropylamineHCID 69828—
Reactant2-Anilino-4-(1-methyl-2-isopropylimidazol-5-yl)pyrimidineHCID 11392223—
SolventMethanolHCID 887—
SolventThionyl ChlorideHCID 24386—
ProductHCID 69314314HCID 6931431492%

Reaction Conditions

Temperature0 °C

Reaction Steps

Chlorosulphonic acid (150 μl, 2.16 mmol) was added dropwise to solution of 2-anilino-4-(1-methyl-2-isopropylimidazol-5-yl)pyrimidine (Method 71; 158 mg, 0.54 mmol) in thionyl chloride (3 ml) cooled at 0° C. and the mixture stirred at 0° C. for 10 minutes then heated at 90° C. for 90 minutes. The volatiles were removed by evaporation and the residue was dried under high vacuum (<2 mmHg) for 1 hour. The resulting solid was placed under nitrogen and a solution of cyclopropylamine (570 μl, 8.1 mmol) in MeOH (3 ml) added. The mixture was stirred for 30 minutes and the volatiles were evaporated in vacuo. Trituration with water results in a solid which was washed water (3×20 ml) collected by filtration and dried under vacuum at 60° C. to yield the title compound (205 mg, 92%) as a solid. NMR: 0.30 (m, 2H), 0.45 (m, 2H), 1.24 (d, 6H), 2.19 (m, 1H), 3.17 (m, 1H), 4.01 (s, 3H), 7.19 (d, 1H), 7.70 (d, 2H), 7.92 (d, 2H), 8.02 (m, 1H), 8.50 (d, 1H), 9.90 (brs, 1H); m/z 413.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442697B2
Source datasetuspto-grants-2008_10
ORD IDord-520c25f9f33f4ea99c34843ac2ce9088
Source noteuspto-grants-2008_10