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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719191Generated: October 30, 2026

Bromoacetonitrile → HCID 10157757, compound

https://huagongshe.com/reaction/719191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetonitrileHCID 11534—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178483817HCID 178483817—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 10157757HCID 10157757—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a suspension of 4-hydroxy-benzo[a]phenazine-11-carboxylic acid (2-dimethylamino-ethyl)-amide: hydrobromide salt (230 mg) in dry N,N-dimethylformamide (3 mL) was added potassium tert-butoxide (175 mg) and then bromoacetonitrile (47 μL). The reaction mixture was heated to 100° C. for 1 hour. The reaction mixture was then cooled, diluted with ethyl acetate, washed with sodium carbonate solution and brine, dried (MgSO4) and the solvent removed in vacuo to provide crude product. This was purified using flash chromatography (silica, 25% MeOH in ethyl acetate) to yield the title compound as a yellow solid (74 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132419B2
Source datasetuspto-grants-2006_11
ORD IDord-89a7693c2e8348218db6817249217a0a
Source noteuspto-grants-2006_11