(3RS)-3-amino-1-ethoxycarbonylmethyl-5-(2-fluorophenyl)-2,3-dihydro-1H-1,4-benzodiazepin-2-one → 5-(2-Fluorophenyl)-2,5-dihydro-3-((((1-methylethyl) amino)carbonyl)amino)-2-oxo-1H-1,4-benzodiazepine-1-acetic acid ethyl ester

HRID 620598Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 620598
[NH2:1][CH:2]1[N:8]=[C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[F:15])[C:6]2[CH:16]=[CH:17][CH:18]=[CH:19][C:5]=2[N:4]([CH2:20][C:21]([O:23][CH2:24][CH3:25])=[O:22])[C:3]1=[O:26]>O1CCCC1>[CH2:24]([O:23][C:21](=[O:22])[CH2:20][N:4]1[C:5]2[CH:19]=[CH:18][CH:17]=[CH:16][C:6]=2[CH:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[F:15])[N:8]=[C:2]([NH:1][C:3]([NH:4][CH:5]([CH3:19])[CH3:6])=[O:26])[C:3]1=[O:26])[CH3:25]

Komponenten

3

Versuchsvorschrift

Equimolar amounts of 3(R,S)-amino-1,3-dihydro-1-ethoxycarbonylmethyl-5-(2-fluorophenyl)-2H-1,4-benzodiazepin-2-one and isoproplylisocyanate were mixed in 8 ml of dry tetrahydrofuran at room temperature. The reaction mixture was allowed to stand for 8 hours and was then filtered. The collected solids were washed with tetrahydrofuran and dried in vacuo over P2O5 to give the analytical product: m.p. 155°-157° C.

Aufarbeitung

  1. filtrationwas then filtered
  2. washThe collected solids were washed with tetrahydrofuran
  3. dry with materialdried in vacuo over P2O5
  4. customto give the analytical product

Quellen und Nachweise

ORD-Eintrag
ord-cde87df2688143729befaef06043eadd
Quelldatensatz
uspto-grants-1989_04
Patentnummer
US04820834

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