HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982922Generated: October 28, 2026
Lithium Hydroxide → Methyl 13-cyclohexyl-6-(carboxy)-5H-indolo[2,1-a][2]benzazepine-10-carboxylate
https://huagongshe.com/reaction/1982922
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | dimethyl 13-cyclohexyl-7H-indolo[2,1-a][2]benzazepine-6,10-dicarboxylate | HCID 11640545 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 13-cyclohexyl-6-(carboxy)-5H-indolo[2,1-a][2]benzazepine-10-carboxylate | HCID 68814066 | 97% |
Reaction Steps
Methyl 13-cyclohexyl-6-(methoxycarbonyl)-7H-indolo[2,1-a][2]benzazepine-10-carboxylate (308 mg, 0.72 mmol) was dissolved in N,N-dimethylformamide (5 mL) and treated with LiOH (173 mg, 7.2 mmol). The mixture was heated at 50° C. for 4 hr, after which the solvent was removed in vacuo. The residue was dissolved in H2O (5 mL) and the resultant mixture was acidified by the addition of a 10% aqueous HCL solution. A precipitate formed which was collected by filtration and air dried to afford the title compound as a bright yellow solid (290 mg, 97%). ESI-MS m/z [M+1]=415.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07541351B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-d68eba62c167451a96ecfe8dd34bef59 |
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| Source note | uspto-grants-2009_06 |
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