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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1517280Generated: October 26, 2026

(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

https://huagongshe.com/reaction/1517280

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2R)-2-(tetrahydro-2H-pyran-2-yloxy)propyl methanesulfonateHCID 59627468—
ReactantMethylamine tetrahydrofuranHCID 66615946—
Reactant6-({4-[(1-methyl-1H-pyrazol-3-yl)amino]quinazolin-6-yl}oxy)pyridin-3-olHCID 68429877—
Product6-[(5-{[(2R)-2-(methylamino)propyl]oxy}pyridin-2-yl)oxy]-N-(1-methyl-1H-pyrazol-3-yl)quinazoline-4-amineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232284B2
Source datasetuspto-grants-2012_07
ORD IDord-db1194c7e04e49bd915eb3a4e5f7428c
Source noteuspto-grants-2012_07