HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961377Generated: October 30, 2026
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → (S)-N-(6-Fluoropyridin-3-yl)-2-methylpyrrolidine-2-carboxamide
https://huagongshe.com/reaction/1961377
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-Amino-2-fluoropyridine | HCID 819440 | — |
| Reactant | (2S)-1-(tert-Butoxycarbonyl)-2-methylpyrrolidine-2-carboxylic acid | HCID 11206950 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | (S)-N-(6-Fluoropyridin-3-yl)-2-methylpyrrolidine-2-carboxamide | HCID 59436446 | — |
Reaction Steps
To a stirred solution of (5)-1-(tert-butoxycarbonyl)-2-methylpyrrolidine-2-carboxylic acid (1.0 g, 4.37 mmol) and 6-fluoropyridin-3-amine (1.47 g, 13.1 mmol), 1-hydroxybenzotriazole (0.65 mg, 4.81 mmol), and N-(3-dimethylaminopropyl)-N′-ethyl-carbodiimide (2.5 g, 13.1 mmol) in N-methylpyrrolidinone (10 mL) was added diisopropylethylamine (3.8 mL, 21.8 mmol). The reaction mixture was heated to 65° C. for 12 h and the solvent was evaporated to dryness. The residue was separated by preparative HPLC. The crude product was dissolved in methanol and 4N HCl in dioxane (4 mL) was added. The reaction mixture was stirred at room temperature overnight and the crude product was used in the next step without further purification. LC/MS [M+H]+: 224; Ret time (Method F): 0.78 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08415340B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-0e5787db47444ff19c26f8631e4f81a0 |
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| Source note | uspto-grants-2013_04 |
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