Bromomethylcyclopropane → 2,3,4,5-tetrahydro-1H-1,5-benzodiazepine
Reaktionsgleichung
O=[C:2]1[NH:8][C:7]2[CH:9]=[CH:10][CH:11]=[CH:12][C:6]=2[NH:5][C:4](=O)[CH2:3]1.BrCC1CC1>>[NH:5]1[C:6]2[CH:12]=[CH:11][CH:10]=[CH:9][C:7]=2[NH:8][CH2:2][CH2:3][CH2:4]1Komponenten
3
Versuchsvorschrift
2,4-Dioxo-1,5-bis-cyclopropylmethyl)-2,3,4,5-tetrahydro-1H-1,5-benzodiazepine was prepared following General Procedure 8-M using the product from Example 8-P, Step A, and (bromomethyl)cyclopropane (Lancaster). Purification was by flash chromatography eluting with EtOAc/hexanes (3:7 gradient to straight EtOAc), then recrystallization from EtOAc/hexanes.
Aufarbeitung
- customPurification
- washeluting with EtOAc/hexanes (3:7 gradient to straight EtOAc)
- customrecrystallization from EtOAc/hexanes
Quellen und Nachweise
- ORD-Eintrag
- ord-03a25caae3a44a6f8640ed336cd0ef0e
- Quelldatensatz
- uspto-grants-2008_06
- Patentnummer
- US07390801B2
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