HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrolidine → pyrrolidino-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 5,11-Dihydro-11-ethyl-5-methyl-2-trifluoromethanesulfonyloxy-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one | HCID 10716083 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | pyrrolidino-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one | HCID 131718781 | — |
Reaction Steps
5,11-Dihydro-11-ethyl-5-methyl-2-trifluoromethanesulfonyloxy-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one (0.25 g) was dissolved in pyrrolidine (1 ml) and refluxed 30 min. The cooled solution was diluted with ethyl acetate, washed with water, and the organic phase was dried (anhydrous magnesium sulfate) and concentrated. The resulting oily residue was crystallized from ethyl acetate/hexane to provide 0.11 g of 5,11-dihydro-11-ethyl-5-methyl-2-n-(pyrrolidino-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one, m.p. 185°-188° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05366972 |
| Source dataset | uspto-grants-1994_11 |
| ORD ID | ord-fa1bcef2de084958b1cea21000e2dac9 |
| Source note | uspto-grants-1994_11 |