Water → HCID 21887035, compound

HRID 719796Notes

Reaction equation

HRID 719796 reaction equation
[CH2:1]([N:3]=[C:4]=[O:5])[CH3:2].[Cl:6][CH2:7][CH2:8][CH2:9][CH2:10][C:11]([C:13]1[CH:23]=[CH:22][C:16]2[CH2:17][CH2:18][NH:19][CH2:20][CH2:21][C:15]=2[CH:14]=1)=[O:12].O>O1CCCC1>[Cl:6][CH2:7][CH2:8][CH2:9][CH2:10][C:11]([C:13]1[CH:23]=[CH:22][C:16]2[CH2:17][CH2:18][N:19]([C:4]([NH:3][CH2:1][CH3:2])=[O:5])[CH2:20][CH2:21][C:15]=2[CH:14]=1)=[O:12]

Participants

5

Reactant 3

HCID 962WaterHCID 8022Ethyl isocyanateHCID 21887245HCID 21887245, compound

Product 1

HCID 21887035HCID 21887035, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

Ethyl isocyanate (781 μl) was added to a solution of 5-chloro-1-(2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl)-1-pentanone (2.3 g) obtained in Reference Example 121 in tetrahydrofuran (30 ml). After stirring at room temperature for 60 minutes, water (50 g) was added, extracted with ethyl acetate, and washed with brine. The organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to give a colorless solid (2.2 g).

Workup

  1. extractionextracted with ethyl acetate
  2. washwashed with brine
  3. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  4. customthe solvent was evaporated under reduced pressure

Sources & evidence

ORD record
ord-73a065bdbab34c8db3b991cd399c424a
Source dataset
uspto-grants-2006_11
Patent number
US07132547B2

Reaction notes

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