HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375985Generated: October 29, 2026
Ethyl Acetate → methyl 6-{[(3R)-1-benzyl-3-pyrrolidinyl]amino}nicotinate
https://huagongshe.com/reaction/2375985
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 6-chloropyridine-3-carboxylate | HCID 254249 | — |
| Reactant | (3R)-1-benzylpyrrolidin-3-amine | HCID 1519354 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | methyl 6-{[(3R)-1-benzyl-3-pyrrolidinyl]amino}nicotinate | HCID 68960481 | 68.2% |
Reaction Steps
A mixture of methyl 6-chloronicotinate (8.0 g), (3R)-(−)-1-benzyl-3-aminopyrrolidine (9.86 g), CuO (371 mg) and K2CO3 (8.38 g) in DMF (60 ml) was stirred at 100° C. for 10 hours under atmospheric pressure of nitrogen. The reaction mixture was poured into a mixture of AcOEt and water and the organic layer was washed with brine and dried over MgSO4. The solvent was evaporated in vacuo and the residue was chromatographed on silicagel eluting with AcOEt-MeOH (97:3). The eluted fractions containing the desired product were collected and evaporated in vacuo to give methyl 6-{[(3R)-1-benzyl-3-pyrrolidinyl]amino}nicotinate (9.9 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07465731B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-76e00aa7004547b7a56863a0910cc8cd |
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| Source note | uspto-grants-2008_12 |
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