HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → HCID 54231837, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 19377586 | HCID 19377586 | — |
| Reactant | N-(tert-Butoxycarbonyl)-N-phenylglycine | HCID 21905636 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54231837 | HCID 54231837 | 83% |
Reaction Steps
2.3 g (8.64 mmole) quantity of N,N'-dicyclohexylcarbodiimide was added to 20 ml of a solution of 2.0 g (7.35 mmole) of N-decylpiperazine hydrochloride, 1.9 g (7.56 mmole) of N-t-butoxycarbonylphenylglycine, 1.3 g (15.5 mmole) of sodium hydrogencarbonate and 122 mg (1.0 mmole) of 4-dimethylaminopyridine in anhydrous methylene chloride. The mixture was stirred at room temperature for 12 hours. The precipitated crystals were collected by filtration and washed with methylene chloride. Mother liquor and the washings were combined and concentrated under reduced pressure and the residue was purified by silica gel chromatography (chloroform : methanol =15 : 1), giving 2.8 g (yield: 83 %) of 1-(N-t-butoxycarbonyl-phenylglycyl)-4-decylpiperazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05318970 |
| Source dataset | uspto-grants-1994_06 |
| ORD ID | ord-b0e4ea46eaad49809a7f950ba6b27acc |
| Source note | uspto-grants-1994_06 |