HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → HCID 67334948, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 1-(3,5-Dichlorophenyl)-3-(4-methoxyphenyl)prop-2-yn-1-one | HCID 67335511 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67334948 | HCID 67334948 | — |
Reaction Steps
To a solution of the intermediate from step A (1.13 g, 3.7 mmol) in DMF (20 mL) was added hydrazine (0.37 mL, 4.07 mmol, 35% aqueous solution). After 2 hours the reaction mixture was concentrated in vacuo. The residue was suspended in H2O (20 mL). A white precipitate crashed out. The aqueous layer was extracted with ethyl acetate (2×). The organic layer was dried over anhydrous Na2SO4, filtered and concentrated in vacuo. An off-white solid was obtained. This material was used in the next step without any further purification. 1H NMR (CDCl3, 500 MHz): δ 7.7(d, J=1.8 Hz, 2H), 7.66(d, J=8.4 Hz, 2H), 7.35(s, 1H), 7.03(d, J=8.7 Hz, 2H), 6.8(s, 1H), 3.91(s, 3H). LC-MS: 2.92 min. (M+H)=319.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07572922B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-6bb7f84e63ab46d19659abd44727d5f2 |
| Source note | uspto-grants-2009_08 |