HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(2-Methoxyphenyl)piperazine → 2-{[4-(2-Methoxyphenyl)-1-piperazinyl]methyl}[1,3]thiazolo[5,4-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(2-Methoxyphenyl)piperazine | HCID 1346 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-(Chloromethyl)-[1,3]thiazolo[5,4-b]pyridine | HCID 14204207 | — |
| Product | 2-{[4-(2-Methoxyphenyl)-1-piperazinyl]methyl}[1,3]thiazolo[5,4-b]pyridine | HCID 10405002 | — |
Reaction Steps
The product from Example 38A (200 mg, 1.1 mmol), 1-(2-methoxyphenyl)piperazine (229 mg, 1.2 mmol), and DIEA (380 μL, 2.2 mmol) were processed as described in Example 38B to provide the title compound. 1H NMR (300 MHz, DMSO-d6) δ 2.74 (m, 4H) 3.02 (m, 4H) 3.78 (s, 3H) 4.04 (s, 2H) 6.91 (m, 3H) 7.56 (dd, J=8.31, 4.75 Hz, 2H) 8.33 (dd, J=8.14, 1.70 Hz, 1H) 8.59 (dd, J=4.75, 1.70 Hz, 1H); (ESI) m/z 341 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07057042B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-d0ff49941df0449f95843dc97a9b2d08 |
| Source note | uspto-grants-2006_06 |