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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255838Generated: October 31, 2026

Triphosgene → HCID 24991078, compound

https://huagongshe.com/reaction/1255838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphosgeneHCID 94429—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Amino-5-methylpyridineHCID 2762894—
Reactant(S)-N-(1-(3-aminophenyl)ethyl)-6-chloropyrazin-2-amineHCID 25218447—
SolventDichloromethaneHCID 6344—
ProductHCID 24991078HCID 2499107842%

Reaction Steps

To a vigourously stirred mixture of N-[(1S)-1-(3-aminophenyl)ethyl]-6-chloropyrazin-2-amine (49 mg, 0.2 mmol) and saturated aqueous sodium hydrogen carbonate (1.2 mL) in dichloromethane (1.2 mL) was added triphosgene (20 mg, 0.067 mmol) in one portion and the mixture was stirred for 3 hours. After this time 5-methylpyridin-3-amine (60 mg, 0.55 mmol) was added and the mixture was stirred for 17 hours. The mixture was then diluted with dichloromethane (20 mL) and was washed with brine (20 mL), dried (MgSO4) and concentrated under reduced pressure. The residue was dissolved in ethyl acetate (20 mL) and extracted with dilute aqueous hydrochloric acid (0.5M, 3×15 mL). The combined acidic extracts were basified to pH 5 with solid potassium hydroxide and were then extracted with dichloromethane (3×20 mL). The combined organic extracts were washed with brine (20 mL), dried (MgSO4) and concentrated under reduced pressure to give an orange oil which was purified by passage through a column of Sephadex with methanol as eluant. N-(3-{(1S)-1-[(6-Chloropyrazin-2-yl)amino]ethyl}phenyl)-N′-(5-methylpyridin-3-yl)urea (32 mg, 42%) was obtained as a colourless foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461161B2
Source datasetuspto-grants-2013_06
ORD IDord-1650cc28eacd4b9ebd20fd51d4cb1a1f
Source noteuspto-grants-2013_06