HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 2-{[4-(6-Methyl-2-pyridinyl)-1-piperazinyl]methyl}[1,3]thiazolo[5,4-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(6-Methylpyridin-2-yl)piperazine | HCID 2736946 | — |
| Reactant | 2-(Chloromethyl)-[1,3]thiazolo[5,4-b]pyridine | HCID 14204207 | — |
| Product | 2-{[4-(6-Methyl-2-pyridinyl)-1-piperazinyl]methyl}[1,3]thiazolo[5,4-b]pyridine | HCID 9996435 | — |
Reaction Steps
The product from Example 38A (150 mg, 0.81 mmol), 1-(6-methyl-2-pyridinyl)piperazine (160 mg, 0.98 mmol), and DIEA (280 μL, 1.6 mmol) were processed as described in Example 38B to provide the title compound. 1H NMR 1H NMR (300 MHz, DMSO-d6) δ 2.68 (m, 4H) 3.32 (s, 3H) 3.53 (m, 4H) 4.04 (s, 2H) 6.54 (m, 1H) 6.61 (d, J=8.48 Hz, 1H) 7.40 (m, 1H) 7.56 (dd, J=8.31, 4.58 Hz, 1H) 8.33 (dd, J=8.31, 1.53 Hz, 1H); (ESI) m/z 326 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07235661B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-aec54867c755499398599f3f394f09a9 |
| Source note | uspto-grants-2007_06 |