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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276373Generated: October 31, 2026

2-Amino-5-chloropyridine → HCID 66705878, compound

https://huagongshe.com/reaction/2276373

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-chloropyridineHCID 66174—
ReactantDiisopropylethylamineHCID 81531—
ReactantTriphosgeneHCID 94429—
ReactantTriethylazanium chlorideHCID 12698378—
Reactant5-Chloro-2-isocyanatopyridineHCID 20533139—
Reactant1,1-Dimethylethyl 3-(4-aminophenyl)-1-pyrrolidinecarboxylateHCID 57365069—
SolventDichloromethaneHCID 6344—
Solvent1,1-DichloroethaneHCID 6365—
SolventTriethylamineHCID 8471—
ProductHCID 66705878HCID 6670587838%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred suspension of 2-amino-5-chloro-pyridine (1.01 g) in dichloroethane (20 ml) was added portionwise triphosgene (831 mg). Triethylamine (2.22 ml) was then added dropwise and the mixture was stirred at 50° C. for 1 h. The mixture was then concentrated in vacuo to afford a beige solid containing a mixture of triethylammonium chloride and 5-chloro-2-isocyanato-pyridine. This solid was then added to a stirred solution of (RS)-tert-butyl 3-(4-aminophenyl)pyrrolidine-1-carboxylate (350 mg, CAS 908334-28-1) and N,N-diisopropylethylamine (0.68 ml) in dichloroethane (6 ml) and the resulting mixture was stirred at 60° C. overnight. The mixture was then diluted with dichloromethane and washed with water. The phases were separated and the organic phase was dried over sodium sulphate and concentrated in vacuo. The residue was purified by column chromatography (SiO2; gradient: heptane/EtOAc) to give (RS)-3-{4-[3-(5-chloro-pyridin-2-yl)-ureido]-phenyl}-pyrrolidine-1-carboxylic acid tert-butyl ester (212 mg, 38%) as an off-white solid. MS (ISP): 419.2 ([{37Cl}M+H]+), 417.2 ([{35Cl}M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09132136B2
Source datasetuspto-grants-2015_09
ORD IDord-e1aa8b0cb4d34d5cb5acc0a7b471a382
Source noteuspto-grants-2015_09