HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-methyl-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine → HCID 68413344, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-methyl-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine | HCID 398707 | — |
| Reactant | HCID 59456946 | HCID 59456946 | — |
| Product | HCID 68413344 | HCID 68413344 | — |
Reaction Steps
7-bromo-4-methyl-1,3,4,5-tetrahydro-pyrido[e][1,4]diazepin-2-one (1.67 g, 6.55 mmol) was reduced to give a 1:1 mixture of the title compound and 4-methyl-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine. The mixture was dissolved in acetic acid (12 mL), treated with bromine (1.04 g, 6.5 mmol) and stirred at room temperature overnight. Ether (100 mL) was added and the precipitate was isolated by filtration to yield the title compound as an orange solid (2.04 g, 95%). 1H NMR (300 MHz, DMSO-d6) δ10.23 (s, 1H) 8.16 (d, J=2.3 Hz, 1H), 7.84 (d, J=2.0 Hz, 1H), 6.89 (s, 1H), 4.25-4.48 (m, 2H), 3.54-3.58 (m, 2H), 3.28-3.35 (m, 2H), 2.86-2.87 (m, 3H); MS (ESI) m/e 242 (C9H12BrN3+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08895545B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-14bf2d021858496785f561f1e6b76fd2 |
| Source note | uspto-grants-2014_11 |