HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-(4-chlorobenzyl)-1-(7H-pyrrolo(2,3-d)pyrimidin-4-yl)piperidin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 7H-Pyrrolo(2,3-d)pyrimidine, 4-chloro- | HCID 5356682 | — |
| Reactant | 4-(4-Chlorobenzyl)-piperidin-4-ylamine hydrochloride | HCID 66873031 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 4-(4-chlorobenzyl)-1-(7H-pyrrolo(2,3-d)pyrimidin-4-yl)piperidin-4-amine | HCID 17751819 | 49.3% |
Reaction Steps
A solution of 4-(4-chlorobenzyl)piperidin-4-yl amine hydrochloride (0.060 g, 0.2016 mmol), 4-chloro-7H-pyrrolo[2,3-d]pyrimidine (0.031 g, 0.2016 mmol) and triethylamine (0.140 ml, 1.0079 mmol) in n-butanol (2.0 ml) was heated to 100° C. for 24 hours. Concentration and purification by preparative silica TLC gave a white solid (0.034 g, 49%). LC-MS (LCT) m/z 342 [M+H+], Rt 3.25 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08809336B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-c9c0d31cb26c473ea567fe5288372431 |
| Source note | uspto-grants-2014_08 |