Hydrochloric Acid → 2-(3-(10,11-Dihydro-5h-dibenz[b,f]azepin-5-yl)-1-propyl)-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid hydrochloride

HRID 1166419Notes

Reaction equation

HRID 1166419 reaction equation
C[O:2][C:3]([CH:5]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH2:7][N:6]1[CH2:15][CH2:16][CH2:17][N:18]1[C:24]2[CH:25]=[CH:26][CH:27]=[CH:28][C:23]=2[CH2:22][CH2:21][C:20]2[CH:29]=[CH:30][CH:31]=[CH:32][C:19]1=2)=[O:4].C(O)C.[OH-].[Na+].[ClH:38]>O.O1CCCC1>[ClH:38].[CH:29]1[C:20]2[CH2:21][CH2:22][C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=3[N:18]([CH2:17][CH2:16][CH2:15][N:6]3[CH:5]([C:3]([OH:4])=[O:2])[CH2:14][C:13]4[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=4)[CH2:7]3)[C:19]=2[CH:32]=[CH:31][CH:30]=1

Participants

7

Procedure

A mixture of the above ester (0.80 g, 0.0019 mol), ethanol (5 ml), tetrahydrofuran (5 ml) and 4 N sodium hydroxide (4 ml) was stirred at room temperature for 22 h. Water (50 ml) and concentrated hydrochloric acid (2 ml) were added and the mixture was extracted with ethyl acetate (2×20 ml). The combined organic extracts were washed with brine (10 ml), dried (MgSO4) and concentrated in vacuo. This gave 0.8 g of a solid, which was triturated and washed with ethyl acetate (2×5 ml). Drying in vacuo, afforded 0.6 g (75%) of the title compound as a solid.

Workup

  1. extractionthe mixture was extracted with ethyl acetate (2×20 ml)
  2. washThe combined organic extracts were washed with brine (10 ml)
  3. dry with materialdried (MgSO4)
  4. concentrationconcentrated in vacuo
  5. customThis gave 0.8 g of a solid, which was triturated
  6. washwashed with ethyl acetate (2×5 ml)
  7. customDrying in vacuo

Sources & evidence

ORD record
ord-606e9d9075c14362b08a7944bcc43582
Source dataset
uspto-grants-2003_09
Patent number
US06613791B1

Reaction notes

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