HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600639Generated: October 29, 2026
Sulfuric Acid → ethyl 5,6,7,8-tetrahydro-11-chloro-8-methoxy-4H-azocino [3,2,1-hi]indole-2-carboxylate
https://huagongshe.com/reaction/1600639
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | ethyl 5,6,7,8-tetrahydro-11-chloro-8-hydroxy-4H-azocino [3,2,1-hi]indole-2-carboxylate | HCID 21714297 | — |
| Reactant | Ethyl 3-(3-fluoro-2-methylphenyl)-2-azidopropenoate | HCID 54359158 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | ethyl 5,6,7,8-tetrahydro-11-chloro-8-methoxy-4H-azocino [3,2,1-hi]indole-2-carboxylate | HCID 21714310 | — |
Reaction Steps
The ethyl 5,6,7,8-tetrahydro-11-chloro-8-hydroxy-4H-azocino[3,2,1-hi]indole-2-carboxylate (1.90 g, 6.17 mmol) obtained in Example 23, (a) was added to a mixture of methanol (19 ml) and concentrated sulfuric acid (1.89 g) which had been cooled to 0° C. The reaction mixture was heated to 40° C. and stirred for 1 hour. The reaction mixture was poured into ice water and extracted twice with ethyl acetate, and the extract solution was washed twice with a 5% aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was purified by a silica gel column chromatography (eluent: ethyl acetate/n-hexane=1/99) to obtain 1.96 g of ethyl 5,6,7,8-tetrahydro-11-chloro-8-methoxy-4H-azocino-[3,2,1-hi]indole-2-carboxylate as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05977100 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-4c34563fba53443b9b887d1b4dd1dbb5 |
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| Source note | uspto-grants-1999_11 |
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