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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571839Generated: October 29, 2026

Sodium Carbonate → HCID 86674691, compound

https://huagongshe.com/reaction/571839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant5-Amino-2-chloropyridineHCID 79305—
ReactantTriphosgeneHCID 94429—
ReactantHCID 68325701HCID 68325701—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 86674691HCID 8667469170%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of (+)-(R)-tert-butyl 2-(4-amino-3-methylphenyl)morpholine-4-carboxylate (99 mg) in dichloromethane (3 ml) was added a solution of sodium carbonate (72 mg) in water (3 ml). The reaction mixture was cooled to 0° C. and triphosgene (37 mg) was added. The reaction mixture was then stirred at 0° C. for 1 hour. TLC showed all the starting material had reacted. 6-Chloropyridin-3-amine (48 mg, CAS 5350-93-6) was then added and the reaction mixture was stirred at room temperature for a further hour. 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 70% EtOAc in hexanes) to give (R)-tert-butyl 2-(4-(3-(6-chloropyridin-3-yl)ureido)-3-methylphenyl)morpholine-4-carboxylate (106 mg, 70%) as an off-white solid. MS (ISP): 449.2 ([{37Cl}M+H]+), 447.2 ([{35Cl}M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029370B2
Source datasetuspto-grants-2015_05
ORD IDord-d569b26cfa794cecb7cd4d081d7f2cf6
Source noteuspto-grants-2015_05