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Water → HCID 59909615, compound

HRID 1790423
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Reaction equation

HRID 1790423 reaction equation
[C:1]([O:4][CH2:5][C@H:6]1[C@@H:11]([N:12]2[C:20]3[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=3)[CH2:14][CH2:13]2)[CH2:10][CH2:9][NH:8][CH2:7]1)(=[O:3])[CH3:2].C(N(CC)CC)C.[F:28][C:29]1[CH:37]=[CH:36][C:32]([CH2:33][CH2:34]Br)=[CH:31][CH:30]=1.O>CN(C)C=O.CO>[F:28][C:29]1[CH:37]=[CH:36][C:32]([CH2:33][CH2:34][N:8]2[CH2:9][CH2:10][C@H:11]([N:12]3[C:20]4[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=4)[CH2:14][CH2:13]3)[C@H:6]([CH2:5][O:4][C:1](=[O:3])[CH3:2])[CH2:7]2)=[CH:31][CH:30]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 962WaterHCID 8471TriethylamineHCID 5731534-Fluorophenethyl bromideHCID 59909610HCID 59909610, compound

Product 1

HCID 59909615HCID 59909615, compoundYield 28%

Reagents, catalysts & solvents 2

HCID 887
Methanol
Solvent
HCID 6228DimethylformamideSolvent

Conditions

Temperature
50 °C

Procedure

cis-1-(3-Acetoxymethylpiperidin-4-yl)indoline (280 mg) was dissolved in dimethylformamide (4 ml) and methanol (1 ml). To the resultant solution were added triethylamine (222 mg) and 4-fluorophenethyl bromide (285 mg) followed by stirring at 50° C. for 2 hr. Then the reaction mixture was cooled and water (50 ml) was added thereto. After extracting with ether (50 ml) twice, the organic phase was washed with water (20 ml) twice and a 2 N aqueous solution (50 ml) of sodium hydroxide once and dried over anhydrous magnesium sulfate. Then the solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (hexane/ethyl acetate system) to give the title compound (100 mg) as a colorless oil (yield: 28%).

Workup

  1. temperatureThen the reaction mixture was cooled
  2. extractionAfter extracting with ether (50 ml) twice
  3. washthe organic phase was washed with water (20 ml) twice
  4. dry with materiala 2 N aqueous solution (50 ml) of sodium hydroxide once and dried over anhydrous magnesium sulfate
  5. customThen the solvent was evaporated under reduced pressure
  6. customthe residue was purified by silica gel column chromatography (hexane/ethyl acetate system)

Sources & evidence

ORD record
ord-5bf9346edb7047869aa6abab44bb6ed5
Source dataset
uspto-grants-2006_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07071201B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes