Dimethylamine, hydrochloride → 4-(4-Chlorophenyl)-1-[3-(5,11-dihydro-7-dimethylaminocarbonylmethyloxy[1]benzoxepino[2,3-b]pyridin-5-ylidene)propyl]piperidin-4-ol

HRID 457037Notes

Reaction equation

HRID 457037 reaction equation
[C:1]([CH2:4][O:5][C:6]1[C:11]2[CH2:12][C:13](=[CH:21][CH2:22][CH2:23][N:24]3[CH2:29][CH2:28][C:27]([C:31]4[CH:36]=[CH:35][C:34]([Cl:37])=[CH:33][CH:32]=4)([OH:30])[CH2:26][CH2:25]3)[C:14]3[C:15]([O:20][C:10]=2[CH:9]=[CH:8][CH:7]=1)=[N:16][CH:17]=[CH:18][CH:19]=3)(O)=[O:2].O.ON1C2C=CC=CC=2N=N1.Cl.[CH3:50][N:51](C)[CH2:52]CCN=C=NCC.Cl.CNC>CN(C)C=O.C(Cl)(Cl)Cl.O.C(N(CC)CC)C>[Cl:37][C:34]1[CH:33]=[CH:32][C:31]([C:27]2([OH:30])[CH2:28][CH2:29][N:24]([CH2:23][CH2:22][CH:21]=[C:13]3[C:14]4[C:15](=[N:16][CH:17]=[CH:18][CH:19]=4)[O:20][C:10]4[CH:9]=[CH:8][CH:7]=[C:6]([O:5][CH2:4][C:1]([N:51]([CH3:52])[CH3:50])=[O:2])[C:11]=4[CH2:12]3)[CH2:25][CH2:26]2)=[CH:36][CH:35]=1

Participants

9

Reactant 4

HCID 10473Dimethylamine, hydrochlorideHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 27960291-Hydroxybenzotriazole hydrateHCID 66758567HCID 66758567, compound

Product 1

HCID 667587194-(4-Chlorophenyl)-1-[3-(5,11-dihydro-7-dimethylaminocarbonylmethyloxy[1]benzoxepino[2,3-b]pyridin-5-ylidene)propyl]piperidin-4-olYield 86%

Reagents, catalysts & solvents 4

HCID 962WaterSolventHCID 6212ChloroformSolventHCID 6228DimethylformamideSolventHCID 8471TriethylamineSolvent

Procedure

To a solution of product of example 133 (420 mg) in dimethylformamide (17 ml) were added 1-hydroxybenzotriazol hydrate (250 mg), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (310 mg), dimethylamine hydrochloride (270 mg) and triethylamine (0.45 ml), and the mixture stirred at room temperature for 12 hours. Water and chloroform were added to the reaction mixture, the organic layer was separated and washed with saturated aqueous sodium chloride, and dried with magnesium sulfate. The solvent was distilled off under reduced pressure to give the titled compound (380 mg).

Workup

  1. customthe organic layer was separated
  2. washwashed with saturated aqueous sodium chloride
  3. dry with materialdried with magnesium sulfate
  4. distillationThe solvent was distilled off under reduced pressure

Sources & evidence

ORD record
ord-6aeba2969f024b5abe5000b3e4ae5238
Source dataset
uspto-grants-2007_03
Patent number
US07186729B2

Reaction notes

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