Magnesium orthosilicate → HCID 18917518, compound

HRID 975908Notes

Reaction equation

HRID 975908 reaction equation
[CH:1]1[CH:2]=[CH:3][N:4]2[CH2:10][C:9]3[CH:11]=[CH:12][CH:13]=[CH:14][C:8]=3[NH:7][CH2:6][C:5]=12.C(N(CC)C(C)C)(C)C.[C:24]1([C:44]2[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=2)[C:25]([C:30]([NH:32][C:33]2[CH:41]=[CH:40][C:36]([C:37](Cl)=[O:38])=[CH:35][C:34]=2[O:42][CH3:43])=[O:31])=[CH:26][CH:27]=[CH:28][CH:29]=1.[Si]([O-])([O-])([O-])[O-].[Mg+2].[Mg+2]>C(Cl)Cl>[CH:1]1[CH:2]=[CH:3][N:4]2[CH2:10][C:9]3[CH:11]=[CH:12][CH:13]=[CH:14][C:8]=3[N:7]([C:37]([C:36]3[CH:40]=[CH:41][C:33]([NH:32][C:30]([C:25]4[C:24]([C:44]5[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=5)=[CH:29][CH:28]=[CH:27][CH:26]=4)=[O:31])=[C:34]([O:42][CH3:43])[CH:35]=3)=[O:38])[CH2:6][C:5]=12

Participants

6

Reactant 4

HCID 66225Magnesium orthosilicateHCID 81531DiisopropylethylamineHCID 1554704810,11-Dihydro-5H-benzo[e]pyrrolo[1,2-a][1,4]diazepineHCID 220996544-[([1,1′-Biphenyl]-2-ylcarbonyl)amino]-3-methoxybenzoyl chloride

Product 1

HCID 18917518HCID 18917518, compoundYield 79.1%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Procedure

To a solution of 0.70 g of 10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine and 0.56 g of N,N-diisopropylethylamine in 50 ml of methylene chloride is added 1.35 g of 4-[([1,1'-biphenyl]-2-carbonyl)amino]-3-methoxybenzoyl chloride followed by stirring at room temperature for 18 hours. The reaction mixture is washed with water and saturated aqueous NaHCO3 and the organic layer dried(Na2SO4). The organic layer is passed through hydrous magnesium silicate and the filtrate concentrated in vacuo to give a residue which is dissolved in methylene chloride and passed through a pad of hydrous magnesium silicate two additional times to give upon concentration in vacuo to give 1.5 g of amorphous solid. M+=512.

Workup

  1. washThe reaction mixture is washed with water and saturated aqueous NaHCO3
  2. concentrationthe filtrate concentrated in vacuo
  3. customto give a residue which
  4. customto give upon concentration in vacuo

Sources & evidence

ORD record
ord-37465a1e8dcd4a8cb28bb5fcb7a7fc33
Source dataset
uspto-grants-1997_03
Patent number
US05610156

Reaction notes

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