HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2R)-2-(tetrahydro-2H-pyran-2-yloxy)propyl methanesulfonate → 6-[(5-{[(2R)-2-(methylamino)propyl]oxy}pyridin-2-yl)oxy]-N-(1-methyl-1H-pyrazol-3-yl)quinazoline-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2R)-2-(tetrahydro-2H-pyran-2-yloxy)propyl methanesulfonate | HCID 59627468 | — |
| Reactant | Methylamine tetrahydrofuran | HCID 66615946 | — |
| Reactant | 6-({4-[(1-methyl-1H-pyrazol-3-yl)amino]quinazolin-6-yl}oxy)pyridin-3-ol | HCID 68429877 | — |
| Product | 6-[(5-{[(2R)-2-(methylamino)propyl]oxy}pyridin-2-yl)oxy]-N-(1-methyl-1H-pyrazol-3-yl)quinazoline-4-amine | HCID 59508836 | — |
Reaction Steps
Using 6-({4-[(1-methyl-1H-pyrazol-3-yl)amino]quinazolin-6-yl}oxy)pyridin-3-ol obtained in Example 6-3), (2R)-2-(tetrahydro-2H-pyran-2-yloxy)propyl methanesulfonate and 2 M methylamine/tetrahydrofuran solution, and in the same manner as in Example 26 or according to a method similar to it or according to a combination thereof with an ordinary method, the entitled compound (6 mg) was obtained as a pale yellow amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08232284B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-db1194c7e04e49bd915eb3a4e5f7428c |
| Source note | uspto-grants-2012_07 |