HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 59507737, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | tert-Butyl 4-(5-aminopyridin-2-yl)piperazine-1-carboxylate | HCID 17999304 | — |
| Reactant | HCID 59507478 | HCID 59507478 | — |
| Reactant | HCID 59507888 | HCID 59507888 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 59507737 | HCID 59507737 | — |
Reaction Steps
To tert-butyl 4-(5-(6-(2-aminopyrimidin-5-yl)-2-morpholinopyrimidin-4-ylamino)pyridin-2-yl)piperazine-1-carboxylate (prepared as described in Example 1 from 5-(6-chloro-2-morpholinopyrimidin-4-yl)pyrimidin-2-amine and commercially available tert-butyl 4-(5-aminopyridin-2-yl)piperazine-1-carboxylate, 30 mg, 0.06 mmol) were added 5 mL of 4N HCl in dioxane. After stirring for one hour, the solution was concentrated in vacuo. The residue was dissolved in a 3:1 acetonitrile and water and lyophilized to afford the desired product LC/MS (m/z): 435.2 (MH+), Rt 1.52 minutes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08563549B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-1ddc188735ee4dbca5db7a0c897fd582 |
| Source note | uspto-grants-2013_10 |