Sodium Chloride → N-1-Azabicyclo[2.2.2]oct-3-yl-2-chloroacetamide, monohydrochloride

HRID 5501

반응식

HRID 5501 반응식
[OH-].[K+].Cl.Cl.[NH2:5][CH:6]1[CH:11]2[CH2:12][CH2:13][N:8]([CH2:9][CH2:10]2)[CH2:7]1.[Cl-].[Na+].[Cl:16][CH2:17][C:18](Cl)=[O:19]>O.C(Cl)Cl>[ClH:16].[N:8]12[CH2:13][CH2:12][CH:11]([CH2:10][CH2:9]1)[CH:6]([NH:5][C:18](=[O:19])[CH2:17][Cl:16])[CH2:7]2

참가 물질

7

반응물 4

HCID 5234Sodium ChlorideHCID 6577Chloroacetyl chlorideHCID 14797Potassium HydroxideHCID 197853Quinuclidine, 3-amino-, dihydrochloride

생성물 1

HCID 131716900N-1-Azabicyclo[2.2.2]oct-3-yl-2-chloroacetamide, monohydrochloride수율 144%

시약·촉매·용매 2

HCID 962Water용매HCID 6344Dichloromethane용매2회

실험 절차

Potassium hydroxide (10 g) was added to a solution of 3-aminoquinuclidine dihydrochloride (10.45 g, 0.052 mole) in water (80 ml) saturated with sodium chloride. After stirring for 30 minutes, methylene chloride (75 ml) was added and the layers separated. The aqueous layer was washed with methylene chloride (2×75 ml), and the extracts combined with the methylene chloride layer above; dried over sodium sulfate, filtered, and the volume reduced to 100 ml. A solution of chloroacetyl chloride (3.11 g, 0.0273 mole) in methylene chloride (25 ml) was added dropwise and the mixture stirred overnight. The solvent was removed on a rotary evaporator. The residue was recrystallized from methanol-ethyl acetate to give a white solid (4.7 g), m.p. ca. 189°-195° C. The structure was confirmed by NMR.

후처리

  1. customthe layers separated
  2. washThe aqueous layer was washed with methylene chloride (2×75 ml)
  3. dry with materialdried over sodium sulfate
  4. filtrationfiltered
  5. stirringthe mixture stirred overnight
  6. customThe solvent was removed on a rotary evaporator
  7. customThe residue was recrystallized from methanol-ethyl acetate

출처 및 근거

ORD 기록
ord-0036974a8e5f42138d995cc37559e5bb
출처 데이터셋
uspto-grants-1993_09
특허 번호
US05244899

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