HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 23513730, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 4-(Pyridin-4-yl)benzoic acid | HCID 1520811 | — |
| Reactant | HCID 23513722 | HCID 23513722 | — |
| Reactant | HCID 23513731 | HCID 23513731 | — |
| Product | HCID 23513730 | HCID 23513730 | — |
Reaction Steps
By a method analogous to that described in Example 3 starting from 4-(4-pyridyl)benzoic acid (199 mg, 1 mmol) and 1-(5-bromoindol-2-ylsulphonyl)piperazine (344 mg, 1 mmol, 1 mol eq.), was prepared 1-(5-bromoindol-2-ylsulphonyl)-4-[4-(4-pyridyl)benzoyl]piperazine methane sulphonic acid salt, (155 mg), 1H NMR (d6-DMSO) 2.3 (s, 3H), 3.0-3.3 (broad d, 4H), 3.4-3.8 (broad d, 4H), 7.0 (d, 1H), 7.45 (s, 2H), 7.6 (d, 2H), 7.95 (s, 1H), 8.0 (d, 2H), 8.25 (d, 2H), 8.9 (d, 2H), 12.4 (s, 1H), signals were also present due to ethanol (0.15 mol equiv.); MS (M+H)+ 525/527.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06753331B1 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-c9a618e2e21b4dfc88878161f76a3197 |
| Source note | uspto-grants-2004_06 |