HuagongsheHuagongshe Chemistry Print Report · For research reference only
8-amino-5H-benzo[b][1,4]benzoxazepin-6-one → HCID 178465553, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 8-amino-5H-benzo[b][1,4]benzoxazepin-6-one | HCID 2756399 | — |
| Reactant | 2-Naphthylmethyl ethanimidothioate hydrobromide | HCID 22138705 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178465553 | HCID 178465553 | — |
Reaction Steps
To a stirred solution of 2-amino-10H-dibenzo[b,f][1,4]oxazepin-11-one (Example 4, 50 mg, 0.22 mmol) in 4 mL of ethanol at 0° C. was added thioacetimidic acid naphthalen-2-ylmethyl ester hydrobromide (65 mg, 0.22 mmol). The reaction was warmed to room temperature overnight. The mixture was concentrated at reduced pressure and partitioned between water (5 mL) and ethyl acetate (25 mL). The aqueous layer was separated and evaporated under vacuum (yield 70 mg, 92%). H1 NMR (DMSO d6) δ: 11.15 (bs, 1H), 10.68 (s, 1H), 9.44 (bs, 1H), 8.56 (bs, 1H), 7.71-7.70 (m, 1H), 7.54-7.53 (m, 2H), 7.40-7.36 (m, 1H), 7.20-7.17 (m, 3H), 2.31 (s, 3H), MS (ES): MH+ 268.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06919328B1 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-d1e932c3f07547b5934f1964769a7d45 |
| Source note | uspto-grants-2005_07 |