HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 67364381, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1,1-Dimethylethyl 8-chloro-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepine-5(6H)-carboxylate | HCID 67365494 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67364381 | HCID 67364381 | 85% |
Reaction Steps
N-Bromosuccinimide (4.50 g, 24.0 mmol) was added to 8-chloro-4H,6H-2,3,5,10b-tetraaza-benzo[e]azulene-5-carboxylic acid tert-butyl ester (7.00 g, 21.8 mmol) in tetrahydrofuran (140 ml). The mixture was stirred in boiling tetrahydrofuran for 2 hours. The solvent was removed in vacuo and the residue was purified by chromatography (50 g silica gel, heptane: ethylacetate 1:9 to 1:0) to yield 7.39 g (85%) 1-bromo-8-chloro-4H,6H-2,3,5,10b-tetraaza-benzo[e]azulene-5-carboxylic acid tert-butyl ester as white solid. MS m/e: 401 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08664216B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-b1fdffb1790a4a76999b951b6d7b47b4 |
| Source note | uspto-grants-2014_03 |