HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575329Generated: October 31, 2026
alpha-Bromo-o-chlorotoluene → methyl 10-bromo-3-(2-chlorobenzyl)-9-fluoro-6,7-dihydro-5H-5,7-methanobenzo[c]imidazo[1,2-a]azepine-2-carboxylate
https://huagongshe.com/reaction/575329
Participants
| Role | Name | HCID | Charge |
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| Reactant | alpha-Bromo-o-chlorotoluene | HCID 11905 | — |
| Reactant | Methyl 10-bromo-9-fluoro-6,7-dihydro-5H-5,7-methanobenzo[c]imidazo[1,2-a]azepine-2-carboxylate | HCID 86693079 | — |
| Product | methyl 10-bromo-3-(2-chlorobenzyl)-9-fluoro-6,7-dihydro-5H-5,7-methanobenzo[c]imidazo[1,2-a]azepine-2-carboxylate | HCID 86693363 | — |
Reaction Steps
Methyl 10-bromo-9-fluoro-6,7-dihydro-5H-5,7-methanobenzo[c]imidazo[1,2-a]azepine-2-carboxylate (0.3 g) was reacted with 2-Chlorobenzyl bromide similar to as described in example 8 with non-critical modifications to produce methyl 10-bromo-3-(2-chlorobenzyl)-9-fluoro-6,7-dihydro-5H-5,7-methanobenzo[c]imidazo[1,2-a]azepine-2-carboxylate. This crude intermediate was reacted via General Procedure L to provide 10-bromo-3-(2-chlorobenzyl)-9-fluoro-6,7-dihydro-5H-5,7-methanobenzo[c]imidazo[1,2-a]azepine-2-carboxamide which was reacted as a crude with 2-Methyl-3-butyne-ol via General Procedure E to afford 13 mg (3%) of 3-[(2-chlorophenyl)methyl]-9-fluoro-10-(3-hydroxy-3-methyl-but-1-ynyl)-5,6,7,12-tetrahydro-5,7-methanobenzo[c]imidazo[1,2-a]azepine-2-carboxamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09034866B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-79507c52ab8e41ccbe262ebdede47774 |
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| Source note | uspto-grants-2015_05 |
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