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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362475Generated: October 26, 2026

5-Amino-2-methylphthalazin-1-one → 5-{[(2R*,4R*)-4-(3-fluoro-2-methoxyphenyl)-2-hydroxy-2-(trifluoromethyl)pentyliden]amino}-2-methylphthalazin-1-one

https://huagongshe.com/reaction/1362475

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Amino-2-methylphthalazin-1-oneHCID 17985045—
Reactant(2R*,4R*)-4-(3-fluoro-2-methoxyphenyl)-2-hydroxy-2-(trifluoromethyl)pentanalHCID 25180225—
CatalystTitanium tetraethoxideHCID 76524—
Product5-{[(2R*,4R*)-4-(3-fluoro-2-methoxyphenyl)-2-hydroxy-2-(trifluoromethyl)pentyliden]amino}-2-methylphthalazin-1-oneHCID 68775860—

Reaction Steps

In the same way as in Example 1, 295 mg (1.0 mmol) of (2R*,4R*)-4-(3-fluoro-2-methoxyphenyl)-2-hydroxy-2-(trifluoromethyl)pentanal, 217 mg (1.0 mmol) of 5-amino-2-methylphthalazin-1-one and 0.53 ml of titanium tetraethoxide are reacted to give 5-{[(2R*,4R*)-4-(3-fluoro-2-methoxyphenyl)-2-hydroxy-2-(trifluoromethyl)pentyliden]amino}-2-methylphthalazin-1-one. 590 mg of resultant crude imine are cyclized, in the same way as in Example 1, at −30° C. using 10 ml (10 mmol) of 1 M boron tribromide solution to give the desired product. Column chromatography on silica gel (hexane/ethyl acetate 0-60%) yields 204 mg of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880042B2
Source datasetuspto-grants-2011_02
ORD IDord-2f9db710d2be40d79f347281b6b8ea34
Source noteuspto-grants-2011_02