HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2-(3-(2-(1-isopropyl-1H-1,2,4-triazol-5-yl)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepin-9-yl)azetidin-1-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 2-Bromoacetamide | HCID 69632 | — |
| Reactant | 8-Azetidin-3-yl-2-(2-isopropyl-2H-[1,2,4]triazol-3-yl)-4,5-dihydro-6-oxa-1,3a-diaza-benzo[e]azulene hydrochloride | HCID 67050665 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(3-(2-(1-isopropyl-1H-1,2,4-triazol-5-yl)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepin-9-yl)azetidin-1-yl)acetamide | HCID 58204424 | — |
Reaction Steps
Following the procedure for 143, 8-azetidin-3-yl-2-(2-isopropyl-2H-[1,2,4]triazol-3-yl)-4,5-dihydro-6-oxa-1,3a-diaza-benzo[e]azulene hydrochloride (Example 65) was reacted with bromo acetamide. The crude product was subjected to flash chromatography (SiO2, gradient 0 to 10% MeOH in DCM) then trituration in diethyl ether to give 192 as a white solid. 1H NMR δ (ppm) (CDCl3): 8.46 (1 H, d, J=8.28 Hz), 7.84 (1 H, s), 7.61 (1 H, s), 7.07 (1 H, dd, J=8.32, 1.84 Hz), 6.95 (1 H, d, J=1.79 Hz), 6.89 (1 H, s), 5.99-5.90 (1 H, m), 5.44 (1 H, s), 4.48-4.45 (2 H, m), 4.43-4.40 (2 H, m), 3.86-3.78 (2 H, m), 3.73-3.63 (1 H, m), 3.38-3.31 (2 H, m), 3.20 (2 H, s), 1.56 (6 H, d, J=6.64 Hz). LCMS: RT=5.45 min, M+H+=408
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09198918B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-134a2eeab3a249ec893fb0e858989c82 |
| Source note | uspto-grants-2015_12 |