methyl (7R)-7-azido-14-cyclohexyl-7,8-dihydro-6H-indolo[1,2-e][1,5]benzoxazocine-11-carboxylate → Methyl(7r)-7-amino-14-cyclohexyl-7,8-dihydro-6h-indolo[1,2-e][1,5]benzoxazocine-11-carboxylate

HRID 1714016Notes

Reaction equation

HRID 1714016 reaction equation
[N:1]([C@@H:4]1[CH2:11][N:10]2[C:12]3[CH:13]=[C:14]([C:25]([O:27][CH3:28])=[O:26])[CH:15]=[CH:16][C:17]=3[C:18]([CH:19]3[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]3)=[C:9]2[C:8]2[CH:29]=[CH:30][CH:31]=[CH:32][C:7]=2[O:6][CH2:5]1)=[N+]=[N-]>CO.[Pd]>[NH2:1][C@@H:4]1[CH2:11][N:10]2[C:12]3[CH:13]=[C:14]([C:25]([O:27][CH3:28])=[O:26])[CH:15]=[CH:16][C:17]=3[C:18]([CH:19]3[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]3)=[C:9]2[C:8]2[CH:29]=[CH:30][CH:31]=[CH:32][C:7]=2[O:6][CH2:5]1

Participants

4

Procedure

A solution of the foregoing product from Step 2 in MeOH (0.1 M) containing palladium on charcoal (10%, w/w) was stirred under hydrogen at atmospheric pressure for 4 h. The catalyst was filtered off and the solution was concentrated to dryness under reduced pressure to afford the title compound (92%) MS (ES+) m/z 405 (M+H)+. MS (ES+) m/z 405 (M+H)+; %; [α]D20=+46.4 (c=1, CHCl3).

Workup

  1. filtrationThe catalyst was filtered off
  2. concentrationthe solution was concentrated to dryness under reduced pressure

Sources & evidence

ORD record
ord-52545b78de6645aeb21218375c17d061
Source dataset
uspto-grants-2010_09
Patent number
US07795247B2

Reaction notes

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