HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 25242487, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 57502416 | HCID 57502416 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 25242487 | HCID 25242487 | — |
Reaction Steps
tert-butyl 4-{6-[5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl]pyrazin-2-yl}piperazine-1-carboxylate (0.047 g, 0.10 mmol) was suspended in dioxane (1.0 ml). 4M HCl in dioxane (1.0 ml) was added, and the reaction mixture was stirred at room temperature for 45 min. The reaction mixture was filtered to afford 5-(1-methyl-1H-pyrazol-4-yl)-3-(6-piperazin-1-ylpyrazin-2-yl)-1H-pyrrolo[2,3-b]pyridine as an orange/yellow solid (hydrochloride salt). 1H NMR (600 MHz, DMSO-D6) 12.4 (br s, 1H); 9.41 (br s, 2H); 8.71 (br d, 1H); 8.56 (s, 1H); 8.55 (d, 1H); 8.39 (d, 1H); 8.19 (s, 1H); 8.18 (s, 1H); 7.89 (s, 1H); 3.93 (br t, 4H); 3.87 (s, 3H); 3.25 (br m, 4H). LRMS calculated for C19H20N8 [M+H]+, 361.2; found 361.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08183245B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-2aa3c08e10bf44bc9d876d1a95d45627 |
| Source note | uspto-grants-2012_05 |