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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119320Generated: November 1, 2026

Dimethyl Sulfoxide → HCID 22386456, compound

https://huagongshe.com/reaction/2119320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantN-(3-bromo-4-methylphenyl)-4-(pyridin-4-ylmethyl)phthalazin-1-amineHCID 6918616—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 22386456HCID 22386456—

Reaction Steps

A mixture of 1.22 g (3 mmol) 1-(3-brom-4-methyl-anilino)-4-(4-pyridyl-methyl)-phthalazine (expl. 14 h) and 336 mg (3 mmol) potassium-tert.butylate in 10 ml DMSO is stirred in an open vessel for 10 days at RT. Then the yellow mixture is diluted with EtOAc and water, the aqueous layer separated off and extracted twice with EtOAc. The organic phases are washed twice with water and brine, dried (Na2SO4) and partly concentrated. After adding 10 g of SiO2, the residue is dried in vacuo and the resulting powder put on top of a SiO2 -column. Eluation with dichloromethane/EtOAc (5:1→1:1→EtOAc) yields [4-(3-brom-4 -methyl-anilino)phthalazin-1-yl](pyridin-4-yl)ketone (A) followed by [4-(3-brom-4-methyl-anilino)phthalazin-1-yl](pyridin-4-yl)methanol (B). A: m.p. 249-250° C.; FAB MS (M+H)+=419/421. B: m.p. 240° C.; FAB MS (M+H)+=421/423.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06686347B2
Source datasetuspto-grants-2004_02
ORD IDord-08f6603a8d714c798d9267e8807d66ad
Source noteuspto-grants-2004_02