Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375268Generated: November 2, 2026

Hydrochloric Acid → HCID 24887749, compound

https://huagongshe.com/reaction/2375268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantDiethylmethylamineHCID 12022—
ReactantChlorosulfonic acidHCID 24638—
ReactantEthoxyethylamineHCID 66970—
ReactantHCID 22273557HCID 22273557—
SolventMethanolHCID 887—
SolventThionyl ChlorideHCID 24386—
ProductHCID 24887749HCID 2488774947%

Reaction Conditions

Temperature0 °C

Reaction Steps

Chlorosulphonic acid (280 μl, 4 mmol) was added dropwise to solution of 2-anilino-4-(1-ethyl-2-methylimidazol-5-yl)pyrimidine (Method 30; 279 mg, 1 mmol) in thionyl chloride (5 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 2-ethoxyethylamine (356 mg, 4 mmol) and diethylmethylamine (1 ml, 15 mmol) in MeOH (3 ml) added. The mixture was stirred for 15 minutes and the volatiles were evaporated in vacuo. Water (20 ml) was added and extracted DCM (2×25 ml). DCM was dried and evaporated in vacuo. The residue was purified by flash chromatography on silica gel eluting with DCM:MeOH (100:0 increasing in polarity to 97:3) to yield a white foam. The white foam was dissolved in MeOH (3 ml) and treated with 1M HCl in ether (0.55 ml, 0.55 mmol). The solvent was evaporated in vacuo and the resultant solid triturated with ether, collected by filtration and dried-under vacuum at 60° C. to yield the title compound (128 mg, 47%) as a yellow solid. NMR: 1.05 (t, 3H), 1.30 (t, 3H), 2.76 (s, 3H), 2.88 (m, 2H), 3.32 (m, 4H), 4.76 (m, 2H), 7.37 (d, 1H), 7.52 (m, 1H), 7.73 (d, 2H), 7.90 (d, 2H), 8.43 (s, 1H), 8.65 (d, 1H), 10.14 (brs, 1H); m/z 431.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465728B2
Source datasetuspto-grants-2008_12
ORD IDord-3dfcdb853d2f42eeb2f159ab9b13dee2
Source noteuspto-grants-2008_12