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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571828Generated: October 30, 2026

Sodium Carbonate → HCID 71086859, compound

https://huagongshe.com/reaction/571828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant3-AminobenzonitrileHCID 16702—
ReactantTriphosgeneHCID 94429—
ReactantHCID 86674686HCID 86674686—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 71086859HCID 7108685942.4%

Reaction Steps

To a stirred solution of tert-butyl (RS)-2-(4-amino-3-cyanophenyl)morpholine-4-carboxylate (70 mg, example 28b) in dichloromethane (2 ml) was added triphosgene (25 mg). A solution of sodium carbonate (49 mg) in water (2 ml) was then added. The reaction mixture was stirred at room temperature for 3 hours. TLC showed all the starting material had reacted. 3-Aminobenzonitrile (28 mg, CAS 2237-30-1) was then added and the reaction mixture was stirred at room temperature for a further 40 hours. TLC showed the reaction was complete. The reaction mixture was poured into dichloromethane and extracted with water. The organic phase was separated, dried over sodium sulphate and concentrated in vacuo. The residue was purified by column chromatography (SiO2; gradient: 0% to 100% EtOAc in hexanes) to give (RS)-2-{3-cyano-4-[3-(3-cyano-phenyl)-ureido]-phenyl}-morpholine-4-carboxylic acid tert-butyl ester (16 mg, 16%) as a white solid. MS (ISP): 392.2 ([M+H—C4H8]+), 348.2 ([M+H—C4H8—CO2]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029370B2
Source datasetuspto-grants-2015_05
ORD IDord-95ecaefb4cfd4daea11844f12515143e
Source noteuspto-grants-2015_05