Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cyclohexyl isocyanate | HCID 18502 | — |
| Reactant | HCID 15427667 | HCID 15427667 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 9863658 | HCID 9863658 | 37.1% |
Reaction Steps
A mixture of cyclohexylisocyanate (100 mg; 0.9 mmol), 3-(3-pyridyl)-1-propyl (2S)-pyrrolidine-2-carboxylate (200 mg; 0.9 mmol) and triethylamine (90 mg; 0.9 mmol) in 20 mL of methylene chloride was stirred for 1 hour and then partitioned between water and a 1:1 mixture of ethyl acetate and hexane. The organic phase was dried, concentrated and purified by column chromatography (50% ethyl acetate/hexane) to obtain 120 mg (36%) of the compound of Example 4 (4, Table I), 1H NMR (CDCl3, 300 MHz): δ1.10-1.27 (m, 6H); 1.69-1.75 (m, 4H); 1.94-2.03 (m, 4H); 2.67-2.73 (t, 2H); 3.31-3.44 (m, 3H); 4.12-4.16 (m, 2H); 4.39-4.42 (m, 1H); 7.25-7.34 (m, 1H); 7.25-7.55 (dd, 1H); 8.45 (s, 2H). Anal. Calcd. for C20H29N3O3—0.6 H2O: C, 64.88; H, 8.22; N, 11.35. Found: C, 64.60; H, 8.18; N, 11.21.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06242468B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-eb1f86229b674dc9b9a9a1f8a54b11cb |
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| Source note | uspto-grants-2001_06 |
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