HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158735Generated: October 26, 2026
2-amino-9-(2-methylprop-2-en-1-yl)-9H-pyrido[2,3-b]indole-3-carboxamide → 2-amino-9-isobutyl-9H-pyrido[2,3-b]indole-3-carboxamide
https://huagongshe.com/reaction/1158735
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-amino-9-(2-methylprop-2-en-1-yl)-9H-pyrido[2,3-b]indole-3-carboxamide | HCID 59513643 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-amino-9-isobutyl-9H-pyrido[2,3-b]indole-3-carboxamide | HCID 24900870 | 65% |
Reaction Steps
2-Amino-9-(2-methylprop-2-en-1-yl)-9H-pyrido[2,3-b]indole-3-carboxamide (xii-a, 143 mg) was dissolved in ethanol (40 mL) and placed under an argon atmosphere. 10% Palladium on carbon (26 mg) was added and the reaction placed under an atmosphere of hydrogen by repeated evacuation followed by back-filling using a balloon filled with hydrogen gas. The reaction stirred for 16 h at room temperature then the catalyst was removed by filtration through Celite® and the filtrate concentrated in vacuo. The residue was purified by silica gel chromatography (5% methanol in methylene chloride) to afford the title compound (44, 44 mg, 65%). NH4OAc standard conditions. DAD Retention time =7.45 min. M+H=283. 1H NMR (300 MHz, CDCl3): Δ 8.22 (s, 1H), 7.83 (d, J=7.3 Hz, 1H), 7.30-7.36 (m, 3H), 7.21 (br s, 1H), 6.66 (br s, 1H), 5.67 (br s, 1H), 4.07 (d, J=7.3 Hz, 1H), 2.28-2.42 (m, 1H), 0.94 (d, J=6.7 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07812018B2 |
|---|
| Source dataset | uspto-grants-2010_10 |
|---|
| ORD ID | ord-7b781a7c9e0a46dab5b66ca58566ea8d |
|---|
| Source note | uspto-grants-2010_10 |
|---|