Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 71285035 | HCID 71285035 | — |
| Product | HCID 71284603 | HCID 71284603 | 59.3% |
Reaction Steps
To tert-butyl-8-(3-ethyl-6-methoxy-5-(methoxycarbonyl)pyridin-2-yl)-3,4-dihydropyrazino[1,2-a]indole-2(1H)-carboxylate (50 mg, 0.11 mmol) was added 6M HCl (1 mL) and the reaction mixture was heated to 80° C. for 1 h. The reaction mixture was then cooled to room temperature and concentrated to afford a crude residue that was triturated with Et2O. The precipitate was filtered and rinsed with Et2O to afford the title compound as a brown solid (22 mg, 50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409905B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-6c19175df6244140b98415634b0f4c26 |
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| Source note | uspto-grants-2016_08 |
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