Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 13376760 | HCID 13376760 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13376761 | HCID 13376761 | — |
Reaction Steps
Aged N-bromosuccinimide (4.89 g, 27.5 mmol) was added in small portions (over 15 min) to a solution of 2-bromo-10-methyl-6,7,8,9-tetrahydropyrido[1,2-a]indol-9-one (described in Example 8, 5.0 g) in methylene chloride (100 mL) and stirring at room temperature was continued for 30 min. This crude mixture was then protected against light, and a solution of bromine (2 mL) in methylene chloride (200 mL) was added very slowly from a dropping funnel. The reaction mixture was washed successively with cold water, 5% sodium bicarbonate, and water again. After drying (MgSO4) and filtration, the solvent was evaporated, and the title compound was crystallized from chloroform, mp 156° C.; yield 6.6 g; Anal. Calcd for C13H11Br2NO: C, 43.72% H, 3.10% N, 3.92% and Found: C, 43.35% H, 3.00% N, 3.99%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04515949 |
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| Source dataset | uspto-grants-1985_05 |
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| ORD ID | ord-4dfd30e928884a6ead85bf5ff48f4b99 |
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| Source note | uspto-grants-1985_05 |
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