Sodium Hydroxide → 7-chloro-6-(3-fluoro-4-methoxycarbonyl-benzylamino)-2,3,4,5-tetrahydro-1H-benzo[d]azepine

HRID 911630Notes

Reaction equation

HRID 911630 reaction equation
[OH-].[Na+].[Cl:3][C:4]1[CH:20]=[CH:19][C:7]2[CH2:8][CH2:9][N:10](C(=O)C(F)(F)F)[CH2:11][CH2:12][C:6]=2[C:5]=1[NH:21][CH2:22][C:23]1[CH:28]=[CH:27][C:26]([C:29]([O:31][CH3:32])=[O:30])=[C:25]([F:33])[CH:24]=1>O1CCOCC1.O>[Cl:3][C:4]1[CH:20]=[CH:19][C:7]2[CH2:8][CH2:9][NH:10][CH2:11][CH2:12][C:6]=2[C:5]=1[NH:21][CH2:22][C:23]1[CH:28]=[CH:27][C:26]([C:29]([O:31][CH3:32])=[O:30])=[C:25]([F:33])[CH:24]=1

Participants

5

Procedure

Add 1M aqueous NaOH (2.8 mL, 2.8 mmol) to a solution of 7-chloro-6-(3-fluoro-4-methoxycarbonyl-benzylamino)-3-(2,2,2-trifluoroacetyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepine (1.31 g, 2.86 mmol) in 1,4-dioxane (13.3 mL) and water (2.6 mL) at 11° C. Allow mixture to warm to room temperature and stir for 1 h. Concentrate in vacuo and partition the residue between dichloromethane (250 mL) and saturated aqueous NaHCO3 (100 mL). Dry the organic phase over Na2SO4, filter and concentrate in vacuo to afford the desired intermediate that was used without further purification.

Workup

  1. concentrationConcentrate in vacuo
  2. custompartition the residue between dichloromethane (250 mL) and saturated aqueous NaHCO3 (100 mL)
  3. dry with materialDry the organic phase over Na2SO4
  4. filtrationfilter
  5. concentrationconcentrate in vacuo

Sources & evidence

ORD record
ord-40fa0259348e4c71a63c2f810480fb30
Source dataset
uspto-grants-2011_09
Patent number
US08022062B2

Reaction notes

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