HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 620579Erstellt: 25. Oktober 2026
1,2-Dichloroethane → 1,3-Dihydro-5-phenyl-3(RS)-(3-trifluoromethylthiobenzoylamino)-2H-1,4-benzodiazepin-2-one
https://huagongshe.com/reaction/620579
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,2-Dichloroethane | HCID 11 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 3-Amino-5-phenyl-1,3-dihydro-1,4-benzodiazepin-2-one | HCID 4259649 | — |
| Edukt | HCID 178526136 | HCID 178526136 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 1,3-Dihydro-5-phenyl-3(RS)-(3-trifluoromethylthiobenzoylamino)-2H-1,4-benzodiazepin-2-one | HCID 20063213 | — |
Reaktionsschritte
3(RS)-Amino-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepin-2-one (80.0 mg, 0.318 mmole), 3-trifluoromethylthiobenzoic acid (70.7 mg, 0.318 mmole), HBT (43.0 mg, 0.318 mmole) and EDC(61.0 mg, 0.318 mmole) were combined in dry DMF (2 ml) and stirred at room temperature. The pH of the mixture was adjusted to 9.0-9.5 with triethylamine (64.4 mg, 0.636 mmole) and the mixture stirred for 10 minutes. The DMF was removed in vacuo, and the residue was treated with 10% citric acid and extracted with EtOAc. The combined organic fractions were washed with sodium carbonate solution, dried over Na2SO4, filtered, and evaporated to dryness in vacuo. The residue was crystallized from EtOAc to give the title compound which was dried in vacuo at 100° C.: (m.p. 230°-232° C.).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04820834 |
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| Quelldatensatz | uspto-grants-1989_04 |
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| ORD ID | ord-a84dfa094c974200a6e96025dbe3a669 |
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| Quellennotiz | uspto-grants-1989_04 |
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