HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22789Generated: October 30, 2026
N-bromobutanimide → HCID 69708076, compound
https://huagongshe.com/reaction/22789
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 69709487 | HCID 69709487 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69708076 | HCID 69708076 | 50% |
Reaction Steps
A dry 25 mL round bottom flask was charged with di(tert-butyl) 8-(2,4-dichlorophenyl)-3,4,4a,9b-tetrahydro-1H-pyrido[4,3-b]indole-2,5-dicarboxylate (0.38 g, 0.74 mmol), DMF (10 mL), N-bromosuccinimide (0.21 g, 1.11 mmol), and stirred at ambient temperature for 18 hours. The reaction was concentrated under high vacuum to remove DMF and partitioned between water and ethyl acetate (2X). The organics were combined, dried with MgSO4, filtered and concentrated to give 461 mg of a crude orange brown oil. Purification of the crude on a 40 gram silica Biotage column using 10% ethyl acetate in heptane gave 217 mg (50%) of di(tert-butyl) 6-bromo-8-(2,4-dichlorophenyl)-3,4,4a,9b-tetrahydro-1H-pyrido[4,3-b]indole-2,5-dicarboxylate as a pale yellow foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06849640B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-a604a07adb6c49008b2d94d2caedc081 |
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| Source note | uspto-grants-2005_02 |
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