HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37947Generated: October 26, 2026
Nitric Acid → 8-Nitro-1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylic acid ethyl ester
https://huagongshe.com/reaction/37947
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Ethyl 1,2,3,6-tetrahydroazepino[4,5-B]indole-5-carboxylate | HCID 57467979 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 8-Nitro-1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylic acid ethyl ester | HCID 66640265 | 8.3% |
Reaction Steps
A solution of nitric acid (90%, 50 μL, 1 mmol) in acetic acid (3 mL) was added dropwise to a stirred solution of ethyl 1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylate (256 mg, 1 mmol) in acetic acid (5 mL) at 10° C. The mixture was allowed to warm to ambient temperature and stirred for another 1.5 hours, then poured into a mixture of ammonium hydroxide and ice and extracted with DCM. The combined extracts was washed with brine, dried with sodium sulfate, and evaporated in vacuo. The crude product was purified by chromatography on silica gel eluting with hexane-EtOAc (75:25) to give 8-nitro-1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylic acid ethyl ester (25 mg); 1H-NMR (CDCl3): δ 11.52 (1H, s), 8.78 (1H, d), 8.43 (1H, m), 7.92 (1H, d), 7.82 (1H, dd), 7.46 (1H, d), 4.24 (2H, q), 3.52 (2H, m), 3.07 (2H, m), 1.27 (3H, t); MS (ES): 301 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524704B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-b2f008b2e465475e8b499cef548de8f9 |
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| Source note | uspto-grants-2013_09 |
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