Water → HCID 58078517, compound

HRID 1696211Notes

Reaction equation

HRID 1696211 reaction equation
[CH3:1][C@@H:2]1[CH2:7][CH2:6][CH2:5][CH2:4][C@@H:3]1[NH:8][C:9]1[C:14]([C:15]([O:17][CH2:18][CH3:19])=[O:16])=[CH:13][N:12]=[C:11]2[NH:20][CH:21]=[CH:22][C:10]=12.[H-].[Na+].Cl[CH2:26][O:27][CH2:28][CH2:29][Si:30]([CH3:33])([CH3:32])[CH3:31].O>CN(C)C=O.CCOC(C)=O>[CH3:1][C@@H:2]1[CH2:7][CH2:6][CH2:5][CH2:4][C@@H:3]1[NH:8][C:9]1[C:14]([C:15]([O:17][CH2:18][CH3:19])=[O:16])=[CH:13][N:12]=[C:11]2[N:20]([CH2:26][O:27][CH2:28][CH2:29][Si:30]([CH3:33])([CH3:32])[CH3:31])[CH:21]=[CH:22][C:10]=12

Participants

7

Procedure

To a solution of ethyl 4-{[(1S,2R)-2-methylcyclohexyl]amino}-1H-pyrrolo[2,3-b]pyridine-5-carboxylate (3.8 g) in N,N-dimethylformamide (76 mL) was added 60% sodium hydride (580 mg) at 4° C. The mixture was stirred at the same temperature for 1 hour. To the mixture was added [2-(chloromethoxy)ethyl](trimethyl)silane (2.55 mL) and the solution was stirred at ambient temperature for 1 hour. To the solution was added water and EtOAc. The mixture was extracted with EtOAc and washed with brine. The extract was dried over MgSO4, filtrated and evaporated. The residue was purified by column chromatography on silica gel with EtOAc and n-hexane (1:3 to 1:1) to give ethyl 4-{[(1S,2R)-2-methylcyclohexyl]amino}-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrrolo[2,3-b]pyridine-5-carboxylate (5.4 g) as a pale yellow oil.

Workup

  1. stirringthe solution was stirred at ambient temperature for 1 hour
  2. extractionThe mixture was extracted with EtOAc
  3. washwashed with brine
  4. dry with materialThe extract was dried over MgSO4
  5. filtrationfiltrated
  6. customevaporated
  7. customThe residue was purified by column chromatography on silica gel with EtOAc and n-hexane (1:3 to 1:1)

Sources & evidence

ORD record
ord-46fc0327184c4c02a5d8cb32cf77522b
Source dataset
uspto-grants-2012_04
Patent number
US08163767B2

Reaction notes

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