HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoylhydrazine → HCID 53258710, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoylhydrazine | HCID 11955 | — |
| Reactant | 5,6-Dihydro-4H-pyrrolo[3,2,1-ij]quinoline-1-carboxylic acid | HCID 22556886 | — |
| Product | HCID 53258710 | HCID 53258710 | — |
Reaction Steps
2-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)-5-phenyl-1,3,4-oxadiazole was synthesized as outlined in General Procedure J using 5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinoline-1-carboxylic acid and benzohydrazide. The crude product was purified using reverse phase chromatography (HPLC, C-18) using trifluoroacetic acid as a modifier to give the desired product 2-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)-5-phenyl-1,3,4-oxadiazole as a yellow solid. Mp=155-157° C.; 400 MHz 1HNMR (DMSO-d6) δ 8.31 (s, 1H), 8.13-8.10 (m, 2H), 7.90 (d, J=8.0 Hz, 1H), 7.65-7.63 (m, 3H), 7.21 (t, J=6.8 Hz, 1H), 7.06 (d, J=7.6 Hz, 1H), 4.31 (t, J=5.6 Hz, 2H), 2.99 (t, J=6.0 Hz, 2H), 2.21-2.18 (m, 2H); LCMS [M+H]: 302.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08563567B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-2ca3aa98d6bd48c7868279e8c7ca0e4a |
| Source note | uspto-grants-2013_10 |