3-Chloroaniline → N-(3-chlorophenyl)-1-oxo-2,3,4,5-tetrahydro-1H-[1,4]diazepino[1,2-a]indole-8-carboxamide

HRID 1748343Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1748343
[O:1]=[C:2]1[C:8]2=[CH:9][C:10]3[CH:11]=[CH:12][C:13]([C:16]([OH:18])=O)=[CH:14][C:15]=3[N:7]2[CH2:6][CH2:5][CH2:4][NH:3]1.F[B-](F)(F)F.N1(OC(=[N+](C)C)N(C)C)C2C=CC=CC=2N=N1.[Cl:41][C:42]1[CH:43]=[C:44]([NH2:48])[CH:45]=[CH:46][CH:47]=1.C(N(CC)CC)C>CN(C=O)C.O>[Cl:41][C:42]1[CH:43]=[C:44]([NH:48][C:16]([C:13]2[CH:12]=[CH:11][C:10]3[CH:9]=[C:8]4[C:2](=[O:1])[NH:3][CH2:4][CH2:5][CH2:6][N:7]4[C:15]=3[CH:14]=2)=[O:18])[CH:45]=[CH:46][CH:47]=1

Komponenten

7

Versuchsvorschrift

To a solution of 1-oxo-2,3,4,5-tetrahydro-1H-[1,4]diazepino[1,2-a]indole-8-carboxylic acid (Intermediate J, 49 mg, 0.2 mmol) in DMF (1 mL) is added [(benzotriazol-1-yloxy)-dimethylamino-methylene]dimethyl-ammonium tetrafluoroborate (TBTU) (77 mg, 0.24 mmol) and the reaction is stirred for 10 minutes. The reaction is then treated with 3-chloro-phenylamine (28 mg, 0.22 mmol) followed by triethylamine (0.10 mL, 0.7 mmol) and is stirred for 16 h. The reaction is poured into water (20 mL) and the resulting solid is filtered. The solid is dried, suspended in MTBE (20 mL) and filtered again to afford the title compound (40 mg, 56%) as an off-white solid.

Aufarbeitung

  1. stirringis stirred for 16 h
  2. filtrationthe resulting solid is filtered
  3. customThe solid is dried
  4. filtrationfiltered again

Quellen und Nachweise

ORD-Eintrag
ord-65e863b81c8d473189a3d06aede1fbdb
Quelldatensatz
uspto-grants-2015_10
Patentnummer
US09150577B2

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