HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → HCID 19880191, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | HCID 19880184 | HCID 19880184 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19880191 | HCID 19880191 | 71.5% |
Reaction Steps
To a solution of 2,5-dichloro-3,4-bis(p-methoxybenzyloxy)benzoic acid (2.02 g: 4.36 mMol.) and 1-hydroxybenzotriazole (648 mg: 1.1 Eq.) in tetrahydrofuran (40 ml) is added dicyclohexylcarbodiimide (990 mg: 1.1 Eq.), and the mixture is stirred at room temperature for 90 minutes. This solution is mixed with N-methylpiperazine (0.66 g: 1.5 Eq.) and stirred at room temperature for 1 hour. The reaction mixture is filtered to remove solid and concentrated under reduced pressure. The residue is purified by silica gel chromatography to give 1-(2,5-dichloro-3,4-bis(p-methoxybenzyloxy)benzoyl)-4-methylpiperazine (1.7 g) from the fraction eluting with 5% methanol-chloroform. Yield: 71%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05143910 |
| Source dataset | uspto-grants-1992_09 |
| ORD ID | ord-7efd69176b7c4e5d920a2052ce44fd81 |
| Source note | uspto-grants-1992_09 |