HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-[4-Amino-4-(4-tert-butyl-benzyl)-piperidin-1-yl]-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl 4-chloro-1H-pyrrolo[2,3-b]pyridine-5-carboxylate | HCID 53438275 | — |
| Reactant | 4-(4-Tert-butyl-benzyl)-piperidin-4-ylamine hydrochloride | HCID 66872537 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 4-[4-Amino-4-(4-tert-butyl-benzyl)-piperidin-1-yl]-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid ethyl ester | HCID 57899178 | 65% |
Reaction Steps
A mixture of 4-chloro-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid ethyl ester (Example 68A) (50 mg, 0.22 mmol), 4-(4-tert-butyl-benzyl)-piperidin-4-ylamine hydrochloride (70.8 mg, 0.22 mmol) and triethylamine (150 μL) in n-butanol (1.5 mL) was irradiated in a microwave reactor (200 W) for 1 hour at 100° C. After cooling, the solvent was evaporated and the residue was purified by column chromatography (EtOAc-MeOH 4:1) to give an off-white solid (63 mg, 65%). LC-MS (LCT2) m/z 436 [M+H+], Rt 5.01 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09006430B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-5f831d1aafff4198b85325167366a9e2 |
| Source note | uspto-grants-2015_04 |