Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diphenyl Ether | HCID 7583 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | 4-(N-Boc-amino)piperidine | HCID 723833 | — |
| Reactant | HCID 136338251 | HCID 136338251 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 136338252 | HCID 136338252 | 21% |
Reaction Steps
To a stirred solution of 5-(5-(6-isopropoxypyrazin-2-yl)-1H-indol-3-yl)-1,3,4-oxadiazol-2(3H)-one (0.25 g, 0.74 mmol) in anhydrous DMF (2.5 mL) was added DIPEA (0.25 mL, 1.48 mmol), Ph2O (125 mg, 0.74 mmol) and tert-butyl piperidin-4-ylcarbamate (0.295 g, 1.4 mmol) sequentially. The reaction was stirred for 5 min, BOP (360 mg, 0.8 mmol) was added and the reaction was further stirred for 12 h at RT. The mixture was diluted with water (25 mL) and the resulting suspension was filtered. The solid was triturated with 50% EtOAc in petroleum ether to give tert-butyl (1-(5-(5-(6-isopropoxypyrazin-2-yl)-1H-indol-3-yl)-1,3,4-oxadiazol-2-yl)piperidin-4-yl)carbamate (80 mg, 21%) as a solid. MS (ESI, pos. ion) m/z: 520.3 (M+1); 1H NMR (400 MHz, DMSO-d6): δ ppm: 12.01 (s, 1H), 8.74 (s, 2H), 8.13 (s, 1H), 8.07 (s, 1H), 7.98 (d, J=8.4 Hz, 1H), 7.63 (d, J=8.4 Hz, 1H), 7.00 (d, J=7.2 Hz, 1H), 5.40-5.46 (m, 1H), 3.73-3.87 (m, 2H), 3.50 (s, 1H), 3.16 (t, J=10.6 Hz, 1H), 2.98 (t, J=9.2 Hz 1H), 1.84 (s, 2H), 1.33 (s, 17H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09090593B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-2af595b49d664212add157024280be99 |
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| Source note | uspto-grants-2015_07 |
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