HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
10-methyl-2,3-dihydro-1H-pyrrolo[2,1-c][1,4]benzodiazepine-5,11(10H,11aH)-dione → 8-Chloro-1,2,3,5,10,11a-hexahydro-10-methyl-11 H-pyrrolo[2,1-c] [1,4] benzodiazepin-11-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 10-methyl-2,3-dihydro-1H-pyrrolo[2,1-c][1,4]benzodiazepine-5,11(10H,11aH)-dione | HCID 9859436 | — |
| Edukt | (+)-8-chloro-1,2,3,11 a-tetrahydro-10-methyl-5 H-pyrrolo[2,1-c] [1,4] benzodiazepin-5,11(10H)-dione | HCID 68145444 | — |
| Produkt | 8-Chloro-1,2,3,5,10,11a-hexahydro-10-methyl-11 H-pyrrolo[2,1-c] [1,4] benzodiazepin-11-one | HCID 68146023 | — |
Reaktionsschritte
This compound is obtained when (+)-8-chloro-1,2,3,11 a-tetrahydro-10-methyl-5 H-pyrrolo[2,1-c] [1,4] benzodiazepin-5,11(10H)-dione (melting point 191° -194°C. prepared from L-proline and 4-chloro-N-methylisatoic anhydride is described in Example 1) is substituted for (+) 1,2,3,11a-tetrahydro-10 -methyl-5 H-pyrrolo[2,1-c] [1,4] benzodiazepin-5,11(10H)-dione in the process of Example 1.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US03947408 |
| Quelldatensatz | uspto-grants-1976_03 |
| ORD ID | ord-992412ba57cf442cb2c356e023131340 |
| Quellennotiz | uspto-grants-1976_03 |