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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Amino-5-chloropyridine | HCID 66174 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | Triethylazanium chloride | HCID 12698378 | — |
| Reactant | 5-Chloro-2-isocyanatopyridine | HCID 20533139 | — |
| Reactant | 1,1-Dimethylethyl 3-(4-aminophenyl)-1-pyrrolidinecarboxylate | HCID 57365069 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 66705878 | HCID 66705878 | 38% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09132136B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-e1aa8b0cb4d34d5cb5acc0a7b471a382 |
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| Source note | uspto-grants-2015_09 |
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