Acetaldehyde → 1-Ethyl-4-[1-(phenylmethoxycarbonyl)-4-piperidinyl]piperidine

HRID 1782720

반응식

HRID 1782720 반응식
[C:1]1([CH2:7][O:8][C:9]([N:11]2[CH2:16][CH2:15][CH:14]([CH:17]3[CH2:22][CH2:21][NH:20][CH2:19][CH2:18]3)[CH2:13][CH2:12]2)=[O:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C([BH3-])#N.[Na+].[CH3:27][C:28]1C=C(C2(C3C=C(Br)C(O)=C(C)C=3)OS(=O)(=O)C3C2=CC=CC=3)C=C(Br)C=1O.C(=O)C>CO.O.CO.Cl>[CH2:27]([N:20]1[CH2:21][CH2:22][CH:17]([CH:14]2[CH2:15][CH2:16][N:11]([C:9]([O:8][CH2:7][C:1]3[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=3)=[O:10])[CH2:12][CH2:13]2)[CH2:18][CH2:19]1)[CH3:28]

참가 물질

8

반응물 4

HCID 177AcetaldehydeHCID 8273Bromocresol PurpleHCID 5003444Sodium cyanoborohydrideHCID 10979576N-Cbz-4,4'-bipiperidine

생성물 1

HCID 183212841-Ethyl-4-[1-(phenylmethoxycarbonyl)-4-piperidinyl]piperidine

시약·촉매·용매 3

HCID 313Hydrochloric Acid용매2회HCID 887Methanol용매HCID 22242641Methanol--water (1/1)용매

실험 절차

To a solution of 18.14 g (0.061 mol) of 1-(phenylmethoxycarbonyl)-4-(4-piperidinyl)piperidine in 450 ml of a methanol/water mixture (1/1 v/v) were added, with stirring, whilst maintaining a temperature of 15 to 20° C., 10.05 g (0.152 mol) of 95% sodium cyanoborohydride and 50 mg of bromocresol purple. Then a solution of 10.57 g (0.24 mol) of acetaldehyde in 50 ml of methanol and 1N hydrochloric acid were alternately added dropwise so that the colour of the mixture changed continuously from blue to yellow. After all had been added and the reaction had finished the mixture was adjusted to pH 2 with hydrochloric acid and extracted twice with 200 ml of diethylether. The aqueous phase was then made alkaline and extracted thoroughly with dichloromethane. The combined dichloromethane extracts were dried over magnesium sulphate and evaporated down in vacuo. The colourless crystallising residue remaining was purified by column chromatography over silica gel (30-60 μm) using FM1 as eluant. Yield of colourless crystals of melting point 93-96° C.: 7.9 g (39.2% of theory).

후처리

  1. additionAfter all had been added
  2. extractionextracted twice with 200 ml of diethylether
  3. extractionextracted thoroughly with dichloromethane
  4. dry with materialThe combined dichloromethane extracts were dried over magnesium sulphate
  5. customevaporated down in vacuo
  6. customThe colourless crystallising residue remaining was purified by column chromatography over silica gel (30-60 μm)

출처 및 근거

ORD 기록
ord-7067cbc152254b86b5c05ae99b72eb8b
출처 데이터셋
uspto-grants-2009_03
특허 번호
US07498325B2

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