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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526133Generated: November 4, 2026

Acetyl chloride → HCID 178475373, compound

https://huagongshe.com/reaction/1526133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantHCID 178419526HCID 178419526—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178475373HCID 1784753739.2%

Reaction Steps

132 μl (1.84 mmol, 145 mg) of acetyl chloride is added in several portions to a suspension of 602 mg (1.18 mmol) of 5-(4-hydroxyphenyl)-1-methyl-9-(piperazin-1-yl)-3H-benzo[f]pyrazolo[3,4-c][2,7]naphthyridin-6(7H)-one hydrobromide in 120 ml of THF at 0° C. The mixture is then stirred for 48 hours at room temperature and then concentrated under reduced pressure. The residue is purified by reverse-phase preparative HPLC to yield 51 mg (8%) of 4-(1-methyl-6-oxo-9-(piperazin-1-yl)-6,7-dihydro-3H-benzo[f]pyrazolo[3,4-c][2,7]naphthyridin-5-yl)phenyl acetate in the form of a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085575B2
Source datasetuspto-grants-2015_07
ORD IDord-992f7b61b0534ac7898998e3b966654d
Source noteuspto-grants-2015_07