HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazomethane → HCID 131713690, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | HCID 137175481 | HCID 137175481 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 131713690 | HCID 131713690 | 99% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04472578 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-b157771422d7417183a4f44519c0f6ad |
| Source note | uspto-grants-1984_09 |