HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
1-Naphthalenesulfonyl chloride → HCID 178453605, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 1-Naphthalenesulfonyl chloride | HCID 66560 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | HCID 178453600 | HCID 178453600 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | HCID 178453605 | HCID 178453605 | — |
Reaktionsschritte
A solution of trans- (4-aminomethyl-cyclohexylmethyl)-carbamic acid tert-butyl ester (17 g) and ethyldiisopropylamine (14.41 ml) in N,N-dimethylformamide (350 ml) is cooled to 0° C. and treated with a solution of naphthalene-1-sulfonylchloride (15.9 g) in N,N-dimethylformamide (100 ml). The reaction is stirred at ambient temperature for 2 h, concentrated in vacuo. The residue is taken up in dichloromethane, washed with a 0.5 N HCl solution, a saturated aqueous sodium carbonate solution and water, dried and concentrated. Crystallization from hexanes-ethyl acetate gives trans-(4-[ (naphthalene-1-sulfonylamino)-methyl]-cyclohexylmethyl)-carbamic acid tert-butyl ester as a white powder, melting at 199-200° C. Rf(A1) 0.42.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06713265B1 |
| Quelldatensatz | uspto-grants-2004_03 |
| ORD ID | ord-b868e4eaa1c24fd189d3b8cf6c59dfb9 |
| Quellennotiz | uspto-grants-2004_03 |