HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Phenylacetonitrile → 2-Amino-5-iodobenzophenone
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Phenylacetonitrile | HCID 8794 | — |
| Edukt | 1-Iodo-4-nitrobenzene | HCID 12495 | — |
| Edukt | 2-Amino-5-chlorobenzophenone | HCID 12870 | — |
| Edukt | Diethyl chlorophosphate | HCID 13139 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Benzodiazepine | HCID 134664 | — |
| Edukt | Ethyl isocyanoacetate | HCID 533707 | — |
| Produkt | 2-Amino-5-iodobenzophenone | HCID 12906640 | — |
Reaktionsschritte
2-Amino-5-iodo-benzophenone was prepared from p-iodonitrobenzene and phenylacetonitrile according to the literature. 2-Amino-5-chloro-benzophenone was commercially available from Acros. The benzodiazepine 60 was reacted with diethylphosphorochloridate in the presence of sodium hydride, followed by the addition of ethyl isocyanoacetate to provide the ester 62 (Hz120), as shown in Scheme 13.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08835424B2 |
| Quelldatensatz | uspto-grants-2014_09 |
| ORD ID | ord-f1662cbb6fb246f4be0376cb71edfe68 |
| Quellennotiz | uspto-grants-2014_09 |