Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Chloro-N,N-2-trimethylpropenylamine | HCID 640792 | — |
| Reactant | 6-Fluoroquinoline-4-carboxylic acid | HCID 18475525 | — |
| Reactant | HCID 89705144 | HCID 89705144 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 71667229 | HCID 71667229 | — |
Reaction Steps
6-Fluoroquinoline-4-carboxylic acid (17) (0.054 g, 0.282 mmol) was dissolved in a 1:1 mixture of dry DCM and THF (5 mL). 1-chloro-N,N,2-trimethylprop-1-en-1-amine (0.052 mL, 0.395 mmol) was added to this solution, and the mixture was stirred for 30 minutes at rt. Then, a solution of (S)-1-(2-aminoacetyl)pyrrolidine-2-carbonitrile 2,2,2-trifluoroacetate (0.075 g, 0.282 mmol) prepared as described in general procedure B and triethylamine (80 μL, 0.571 mmol) in 3 mL dry THF was added, and the mixture was stirred for 2 h. After evaporation of volatiles, the residue was dissolved in DCM (15 mL), washed with saturated sodium bicarbonate and brine. The organic layer was dried over sodium sulfate, filtrated and purified using flash chromatography (95-5 ethyl acetate-methanol) to yield white crystals
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346814B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-b0d19142e60e4fe98e8acfc0cd9842f7 |
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| Source note | uspto-grants-2016_05 |
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