HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → 2-Hydrazino-5,6-dihydrobenzo[h]quinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 2-Chloro-5,6-dihydrobenzo[h]quinazoline | HCID 53486027 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-Hydrazino-5,6-dihydrobenzo[h]quinazoline | HCID 59774515 | — |
Reaction Steps
Crude 2-chloro-5,6-dihydrobenzo[h]quinazoline was heated at 120° C. in a mixture of anhydrous pyridine (20 mL) and anhydrous hydrazine (7 mL) for 4 h. The solvent was removed under vacuum and the residue was partitioned between chloroform and 1M aqueous potassium carbonate solution. The organic layer was dried over anhydrous sodium sulfate and concentrated under vacuum to give 2-hydrazinyl-5,6-dihydrobenzo[h]quinazoline as a white solid, 2.16 g. 1H NMR (CDCl3, 300 MHz) 8.27 (d, 1H), 8.20 (s, 1H), 7.35 (m, 2H), 7.21 (d, 1H), 6.42 (s, 1H), 4.00 (br s, 2H), 2.91 (m, 2H), 2.80 (m, 2H) ppm; 13C NMR (CDCl3, 75 MHz) 164.29, 160.00, 156.72, 139.87, 132.83, 131.02, 128.25, 127.25, 125.47, 119.03, 28.54, 24.24; MS (ES) 213 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09353126B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-d6ba9eb7f87a43808d00ba41e8463c4f |
| Source note | uspto-grants-2016_05 |