HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471331Generated: October 31, 2026
1-Chloro-4-phenylphthalazine → HCID 1386209, compound
https://huagongshe.com/reaction/1471331
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Chloro-4-phenylphthalazine | HCID 272109 | — |
| Reactant | 5-Amino-1-phenylbenzimidazole | HCID 965312 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 1386209 | HCID 1386209 | 99.6% |
Reaction Steps
A solution of 1-chloro-4-phenylphthalazine (156 mg, 0.65 mmol) and 5-amino-1-phenylbenzimidazole (4) (105 mg, 0.5 mmol) in i-PrOH (10 mL) is stirred at 95° C. under argon for 2 h. The reaction mixture is concentrated, diluted with sat. NaHCO3 (15 mL), and extracted with CHCl3 (100 mL). The extract is washed (brine) and dried. After solvent removal at reduced pressure, the residue is purified on silica gel (1% to 9% methanol/ethyl acetate) to give 206 mg (99%) of 5 as an orange solid, mp 265° C. IR 3285, 2842, 1615, 1476 cm−1; 1H NMR (CDCl3) δ 7.45-7.61 (m, 5H, 1-PhH), 7.62-7.77 (m, 6H, 4′-C6H5, 7-BenzimidH), 7.82 (dd, J=8.7, 2.1 Hz, 1H, 6-BenzimidH), 7.86-7.90 (m, 1H, 5′-PhthH), 7.91-7.98 (m, 1H, 6′-PhthH), 8.00-8.08 (m, 1H, 7′-PhthH), 8.50 (d, J=2.1 Hz, 1H, 4-BenzimidH), 8.56 (s, 1H, 2-BenzimidH), 8.72 (d, J=8.7 Hz, 1H, 8′-PhthH), 9.37 ppm (s, 1H, NH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09012217B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-4c937f03d04c4d04957890f17d701a28 |
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| Source note | uspto-grants-2015_04 |
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