N-Methylpiperidine → HCID 53729552, compound

HRID 1900190Notes

Reaction equation

HRID 1900190 reaction equation
CN1CCCCC1.[F:8][C:9]1[CH:25]=[CH:24][C:12]([O:13][C:14]([NH:16][C@H:17]([C:21]([OH:23])=O)[CH:18]([CH3:20])[CH3:19])=[O:15])=[CH:11][CH:10]=1.ClC(OCC(C)C)=O.[C:34]([C:36]1[CH:46]=[CH:45][C:39]([O:40][CH2:41][CH:42]([NH2:44])[CH3:43])=[CH:38][CH:37]=1)#[N:35]>C(Cl)Cl.O>[C:34]([C:36]1[CH:46]=[CH:45][C:39]([O:40][CH2:41][CH:42]([NH:44][C:21](=[O:23])[C@H:17]([CH:18]([CH3:19])[CH3:20])[NH:16][C:14]([O:13][C:12]2[CH:11]=[CH:10][C:9]([F:8])=[CH:25][CH:24]=2)=[O:15])[CH3:43])=[CH:38][CH:37]=1)#[N:35]

Participants

7

Reactant 4

HCID 12291N-MethylpiperidineHCID 62365Isobutyl chloroformateHCID 189727992-(4-Cyanophenoxy)-1-methylethylamineHCID 53689894HCID 53689894, compound

Product 1

HCID 53729552HCID 53729552, compoundYield 22.6%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 6344DichloromethaneSolvent

Conditions

Temperature
-20 °C

Procedure

1.2 g of N-methylpiperidine was added to a solution containing 3.0 g of N-(4-fluorophenoxycarbonyl)-L-valine dissolved in 80 ml of methylene chloride, at -20° C. After the mixture was stirred for 15 minutes at the same temperature, 1.6 g of isobutyl chloroformate was added to the mixture, and stirred for 1 hour at -20° C. 2.3 g of (-)-2-(4-cyanophenoxy)-1-methylethylamine was added to this mixture at -60° C., and then the reaction mixture was allowed to sit and warm naturally to room temperature while being stirred, and was stirred for 20 hours at room temperature. Water was subsequently added to the reaction mixture. After the methylene chloride layer was washed successively with a 5% aqueous solution of sodium bicarbonate and water, the organic layer was dried over anhydrous magnesium sulfate and the methylene chloride was removed under reduced pressure. The obtained crude crystal was purified by column chromatography on silica gel, thus obtaining 1.1 g of the desired product in the form of a white crystal (yield: 23% ).

Workup

  1. additionwas added to the mixture
  2. temperaturewarm naturally to room temperature
  3. stirringwhile being stirred
  4. stirringwas stirred for 20 hours at room temperature
  5. washAfter the methylene chloride layer was washed successively with a 5% aqueous solution of sodium bicarbonate and water
  6. dry with materialthe organic layer was dried over anhydrous magnesium sulfate
  7. customthe methylene chloride was removed under reduced pressure
  8. customThe obtained crude crystal
  9. customwas purified by column chromatography on silica gel

Sources & evidence

ORD record
ord-d617e4be86464e5a8154492eb069fe03
Source dataset
uspto-grants-1996_11
Patent number
US05574064

Reaction notes

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