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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952769Generated: November 2, 2026

HCID 86755723, compound → HCID 23299674, compound

https://huagongshe.com/reaction/1952769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86755723HCID 86755723—
ReactantHCID 86755724HCID 86755724—
CatalystSodium HydroxideHCID 14798—
SolventMethanolHCID 887—
ProductHCID 23299674HCID 23299674—

Reaction Steps

Preparation of (E)-(RS)-2-(2-{3-[5-(2,4-diamino-pyrimidin-5-ylmethyl)-2,3-dimethoxy-phenyl -acryloyl}-1,2-dihydro-phthalazin-1-yl)-2-methyl-propionic acid ##STR14## To the solution of 50 mg of methyl (E)-(RS)-2-(2-{3-[5-(2,4-diamino-pyrimidin-5-ylmethyl)-2,3-dimethoxy-phenyl -acryloyl}-1,2-dihydro-phthalazin-1-yl)-2-methyl-propionate (Example 1.12) in 5 ml of methanol are added 3 drops of 2N sodium hydroxide solution and the mixture is held at reflux for 45 min. Subsequently, the mixture is concentrated, the residue is treated with ice-water and neutralized with 2N hydrochloric acid. The insoluble material is recrystallized from methylene/methanol. 41 mg of (E)-(RS)-2-(2-{3-[5-(2,4-diamino-pyrimidin-5-ylmethyl)-2,3-dimethoxy-phenyl]-acryloyl}-1,2-dihydro-phthalazin-1-yl)-2-methyl-propionic acid are isolated as a colorless solid. M.p=245° C., dec.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06114330
Source datasetuspto-grants-2000_09
ORD IDord-3c641784359441ceae498a298ffe5c38
Source noteuspto-grants-2000_09