Trifluoroacetic acid → HCID 67439980, compound

HRID 2045676Notes

Reaction equation

HRID 2045676 reaction equation
O[CH:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([C:12]([O:14][CH3:15])=[O:13])[CH:10]=2)[NH:5][CH:4]([C:16]2[CH:21]=[CH:20][CH:19]=[C:18]([O:22][C:23]([CH3:29])([CH3:28])[C:24]([O:26][CH3:27])=[O:25])[CH:17]=2)[C:3]1([CH3:31])[CH3:30].C([SiH](CC)CC)C.FC(F)(F)C(O)=O.C(=O)([O-])[O-].[Na+].[Na+]>ClCCl>[CH3:27][O:26][C:24](=[O:25])[C:23]([CH3:29])([O:22][C:18]1[CH:17]=[C:16]([CH:4]2[C:3]([CH3:31])([CH3:30])[CH2:2][C:11]3[C:6](=[CH:7][CH:8]=[C:9]([C:12]([O:14][CH3:15])=[O:13])[CH:10]=3)[NH:5]2)[CH:21]=[CH:20][CH:19]=1)[CH3:28]

Participants

6

Procedure

A mixture of methyl 4-hydroxy-2-(3-(1-methoxy-2-methyl-1-oxopropan-2-yloxy)phenyl)-3,3-dim ethyl-1,2,3,4-tetrahydroquinoline-6-carboxylate (510 mg, 1.19 mmol) and triethylsilane (400 mg, 3.44 mmol) in dichloromethane (6 mL) was stirred and cooled with a ice bath. A solution of trifluoroacetic acid (554 mg, 4.86 mmol) in dichloromethane (6 mL) was added slowly to the mixture. The reaction mixture was treated with sodium carbonate, and stirred for 30 min. The mixture was filtered, and the filtrate was concentrated and purified by column chromatography (silica gel, petroleum ether:ethyl acetate=15:1) to afford 230 mg of methyl 2-(3-(1-methoxy-2-methyl-1-oxopropan-2-yloxy)phenyl)-3,3-dimethyl-1,2,3,4-tetrahydroquinoline-6-carboxylate. (Yield: 47%).

Workup

  1. temperaturecooled with a ice bath
  2. stirringstirred for 30 min
  3. filtrationThe mixture was filtered
  4. concentrationthe filtrate was concentrated
  5. custompurified by column chromatography (silica gel, petroleum ether:ethyl acetate=15:1)

Sources & evidence

ORD record
ord-a82e59fe3c5c4c72af3555f4f2babca3
Source dataset
uspto-grants-2013_11
Patent number
US08586747B2

Reaction notes

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