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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227836Generated: October 25, 2026

(+-)-2-Butanol → B-[2-[4-[(4-Phenyl-1-phthalazinyl)amino]phenoxy]-3-pyridinyl]boronic acid

https://huagongshe.com/reaction/227836

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+-)-2-ButanolHCID 6568—
Reactant1-Chloro-4-phenylphthalazineHCID 272109—
Reactant2-(4-Aminophenoxy)pyridin-3-ylboronic acidHCID 57756261—
SolventHexaneHCID 8058—
ProductB-[2-[4-[(4-Phenyl-1-phthalazinyl)amino]phenoxy]-3-pyridinyl]boronic acidHCID 24856075—

Reaction Conditions

Temperature100 °C

Reaction Steps

2-(4-Aminophenoxy)pyridin-3-ylboronic acid (478 mg, 2.08 mmol), 1-chloro-4-phenylphthalazine (500 mg, 2.08 mmol) and butan-2-ol (4.16 ml, 2.08 mmol) were placed in a sealed tube. The reaction vessel was sealed and the mixture heated to 100° C. After 1 h 45 min, the reaction was cooled to rt. Hexane was added and the precipitated tan solid was filtered off with hexanes. LCMS of the solids indicated product, 2-(4-(4-phenylphthalazin-1-ylamino)phenoxy)pyridin-3-ylboronic acid. MS Calculated for C25H19BN4O: [M]+=434. Found: [M+1]+=435.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560551B2
Source datasetuspto-grants-2009_07
ORD IDord-244bc5c5788f46c08c78a7d4b12da76c
Source noteuspto-grants-2009_07