HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → HCID 22250086, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 22250084 | HCID 22250084 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22250086 | HCID 22250086 | 70.1% |
Reaction Steps
A solution of 2-(7-Chloro-thieno[3,2-b]pyridin-2-yl)-4-methyl-thiazole-5-carbonyl chloride, (0.28 g, 0.85 mmol), dry dichloromethane (1.5 mL), and 1-methylpiperazine (0.21 mL, 1.87 mmol) was stirred at room temperature for four hours. A gas discharge and immediate solution were noted. The reaction mixture was evaporated directly onto silica gel and purified through silica gel chromatography to afford [2-(7-Chloro-thieno[3,2-b]pyridin-2-yl)-4-methyl-thiazol-5-yl]-(4-methyl-piperazin-1-yl)-methanone (0.234 g) in 70% yield. C17H17ClN4OS2: APCI 393.2/395.2 (pos.); 1H NMR (d6-DMSO): δ 8.68 (d, 1H, J=5.4 Hz), 8.32 (s, 1H), 7.64 (d, 1H, J=5.4 Hz), 3.6–3.4 (bm, 4H), 2.38 (s, 3H), 2.4–2.2 (bm, 4H), 2.17 (s, 3H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06995171B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-114577f36e3b40609c07eaf1d0e42ef3 |
| Source note | uspto-grants-2006_02 |