HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 343199Erstellt: 25. Oktober 2026
1,2-Dichloroethane → 2-[1-(Isopropyl-phenyl-carbamoylmethyl)-3-methyl-2,4-dioxo-5-phenyl-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepine-3-yl]acetamide
https://huagongshe.com/reaction/343199
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1,2-Dichloroethane | HCID 11 | — |
| Edukt | Ammonium Hydroxide | HCID 14923 | — |
| Edukt | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Edukt | [1-(isopropyl-phenyl-carbamoylmethyl)-3-methyl-2,4-dioxo-5-phenyl-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-yl]acetic acid | HCID 67696769 | — |
| Edukt | {3-(Benzyloxycarbonyl-methyl)-1-[isopropyl-(4-methoxy-phenyl)-carbamoylmethyl]-2,4-dioxo-5-phenyl-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-yl}acetic acid | HCID 86753587 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-[1-(Isopropyl-phenyl-carbamoylmethyl)-3-methyl-2,4-dioxo-5-phenyl-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepine-3-yl]acetamide | HCID 67700623 | — |
Reaktionsschritte
To a stirring solution of 233 mg (0.47 mmol) of [1-(Isopropyl-phenyl-carbamoylmethyl)-3-methyl-2,4-dioxo-5-phenyl-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-yl]-acetic acid, prepared as in Intermediate 7, in 2 mL DMF is added 98 mg (0.51 mmol, 1.1 equiv) of EDC and 76 mg (0.56 mmol, 1.2 equiv) of HOBT. The resulting solution is stirred 5 min, then 75 mL (0.61 mmol, 1.3 equiv) of a 30% solution of ammonium hydroxide is added. The solution is stirred 2 h at RT, then poured into 30 mL of EtOAc and extracted H2O (1×30 mL) and NaHCO3 (1×30 mL). The organic layer is separated, dried (MgSO4), and the solvent removed in vacuo. Purification of the resulting grey solid via reverse phase MPLC using a C-18 column and 60% acetonitrile/40% H2O with 0.1% TFA as eluent followed by lyophilization afforded 35 mg of the title compound as a white amorphous solid: 1H NMR (CDCl3, 300 MHz, mixture of conformers) δ7.47-6.80 (m, 14H), 6.70 (s, br, 0.5H), 5.84 (s, br, 0.5H), 5.03 (m, 1H), 4.63 (d, 0.5H, J=16.6), 4.35 (d, 0.5H, J=16.3), 4.08 (d, 0.5H, J=16.6), 3.74 (d, 0.5H, J=16.3), 3.10 (m, 1H), 2.46 (d, 0.5H, J=14.7), 2.23 (d, 0.5H, J=14.7), 1.65 (s, 1.5H), 1.16 (m, 7.5H); low resolution MS (FAB)m/e 499 (MH+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05859007 |
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| Quelldatensatz | uspto-grants-1999_01 |
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| ORD ID | ord-7e94392d699b43ec8ebbfd0d678920e6 |
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| Quellennotiz | uspto-grants-1999_01 |
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