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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2418478Generated: November 2, 2026

Diazomethane → HCID 131713690, compound

https://huagongshe.com/reaction/2418478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazomethaneHCID 9550—
ReactantHCID 137175481HCID 137175481—
SolventEthanolHCID 702—
ProductHCID 131713690HCID 13171369099%

Reaction Steps

To a suspension of 100 of 5-hydroxy-N-β-chloroethylbenzo[a]phenazine-6-carboxyamide in 10 ml of ethanol was added an excess amount of diazomethane ethereal solution, followed by stirring at room temperature overnight. The solvent was concentrated under reduced pressure, and the resulting solid was recrystallized from acetic acid to give 103 mg (99% yield) of 5-methoxy-N-β-chloroethylbenzo[a]-phenazine-6-carboxyamide as yellow needles, m.p. 211°-213° C., Anal. Calcd. (%) for C20H16N3O2Cl; C, 65.89; H, 4.29; N, 11.28; Found: C, 65.67; H, 4.41; N, 11.49

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04472578
Source datasetuspto-grants-1984_09
ORD IDord-b157771422d7417183a4f44519c0f6ad
Source noteuspto-grants-1984_09