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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42211Generated: October 30, 2026

Acetic Anhydride → HCID 25065894, compound

https://huagongshe.com/reaction/42211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium borohydrideHCID 4311764—
Reactant6-[4-[4-(Phenylmethyl)-1-phthalazinyl]-1-piperazinyl]-3-pyridinecarbonitrileHCID 25066518—
CatalystNickel DichlorideHCID 24385—
SolventEthanolHCID 702—
ProductHCID 25065894HCID 2506589452%

Reaction Steps

In a 100 ml, round-bottom flask equipped with a stir bar, 6-[4-(4-Benzyl-phthalazin-1-yl)-piperazin-1-yl]-nicotinonitrile (150 mg, 0.362 mmol) is dissolved in anhydrous EtOH (7 mL) followed by the addition of NiCl2 (0.398 mmol). NaBH4 (0.723 mmol) is added in portions and the reaction is stirred for 2 h under a N2 atmosphere. The septum is removed and Ac2O (1.08 mmol) is added. The reaction is capped again and stirred for one additional hour. LC/MS shows full conversion to the acylated product. The reaction is filtered through a Celite pad and rinsed with 50 ml of MeOH. The final compound is purified by preparative HPLC using a C-18 column and propanol as the modifier (85 mg, 52% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536168B2
Source datasetuspto-grants-2013_09
ORD IDord-77962e20c9fa428fa704765a63fae635
Source noteuspto-grants-2013_09