HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzamidine, hydrochloride → HCID 10638748, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzamidine, hydrochloride | HCID 80289 | — |
| Reactant | Pyrimidine, 2,4-bis(4-bromophenyl)- | HCID 10739118 | — |
| Product | HCID 10638748 | HCID 10638748 | 72% |
Reaction Steps
Benzamidine hydrochloride (4.7 g, 0.03 mole) and 1-dimethylamino-3-dimethylimonio-1-(4-bromophenyl)-1-propene perchlorate are allowed to react as described above in Example 4 for the preparation of 2,4-Bis(4-bromophenyl)-pyrimidine. After work-up and recrystallization from CHCl3 :ethyl ether (1:3), 7.2 g (72%) of a white crystalline solid is obtained which melted at 107°-08° C. IR(KBr) 2925, 1597, 1562, 1540, 1427 cm-1. 1H-NMR: (CDCl3) 8.65 (d, 1H, j=5.3 Hz), 8.55-8.52 (m, 2H), 8.02 (d, 2H, j=8.3 Hz), 7.6 (d, 2H, j=8.8 Hz), 7.5-7.46 (m, 3H), 7.44 (d, 1H, j=5.3 Hz). 13C-NMR (CDCl3): 164.6, 162.5, 157.9, 137.6, 135.7, 132.1, 130.8, 128.6, 128.5, 128.2, 125.6, 114.1. MS m/e: 311 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05622955 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-0ce5dc0ab00540e5906c8723dae3842a |
| Source note | uspto-grants-1997_04 |