HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158746Generated: October 31, 2026
HCID 59513633, compound → HCID 24900807, compound
https://huagongshe.com/reaction/1158746
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 59513633 | HCID 59513633 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 24900807 | HCID 24900807 | 86.5% |
Reaction Steps
To a solution of benzyl{(1R)-2-[2-amino-3-(aminocarbonyl)-9H-pyrido[2,3-b]indol-9-yl]-1-methylethyl}carbamate (xxiv-a, 13 mg, 0.031 mmol) in ethanol (10 mL) was added palladium on carbon (10 mg, 0.094 mmol). The reaction mixture was stirred under a hydrogen atmosphere overnight. Solids were removed by filtration and the filtrate was concentrated in vacuo to afford 2-amino-9-[(2R)-2-aminopropyl]-9H-pyrido[2,3-b]indole-3-carboxamide (35, 7.6 mg, 86%). NH4OAc standard conditions. DAD Retention time =4.90 min. M+H=284. 1H NMR (300 MHz, MeOD-d4): Δ 8.66 (s, 1H), 7.90 (d, J=7.7 Hz, 1H) 7.49 (d, J=8.1 Hz, 1H), 7.23 (ddd, J=7.4, 6.9, 1.2 Hz, 1H), 7.17 (ddd, J1=7.8, 7.7, 1.2 Hz, 1H), 4.33 (d, J=6.1 Hz, 2H), 3.63-3.71 (m, 1H), 1.23 (d, J=6.5 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07812018B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-9b31031ff7bf40df8bbdb73a851875b1 |
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| Source note | uspto-grants-2010_10 |
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