HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexylamine → N-cyclohexyl-5-nitro-1H-pyrrolo[2,3-b]pyridin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | 4-Chloro-5-nitro-1H-pyrrolo[2,3-b]pyridine | HCID 58557259 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-cyclohexyl-5-nitro-1H-pyrrolo[2,3-b]pyridin-4-amine | HCID 58557102 | 57% |
Reaction Steps
To a solution of 4-chloro-5-nitro-1H-pyrrolo[2,3-b]pyridine (0.182 g, 0.921 mmol) in DMF (5 mL) was added cyclohexylamine (0.55 g, 5.5 mmol). The reaction mixture was stirred at ambient temperature for about 2 h. The solvent was removed under reduced pressure and EtOAc (100 mL) and water (20 mL) were added. The layers were separated and the organic layer was washed with water (3×25 mL) and brine (20 mL), dried over anhydrous MgSO4, filtered, and concd to give N-cyclohexyl-5-nitro-1H-pyrrolo[2,3-b]pyridin-4-amine (0.20, 57%) as a brown residue: LC/MS (Table 1, Method c) Rt=1.53 min; MS m/z 261 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08426411B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-b00c53c84115435bac3b67aff09387c0 |
| Source note | uspto-grants-2013_04 |