Triethylamine → 3(S)-(3,4-dichlorophenyl)-4-[2-(1,2,3,4-tetrahydro-5-naphthoyl)imidazol-1-yl]butyl 1,2,3,4-tetrahydro-5-naphthoate

HRID 1533066노트

반응식

HRID 1533066 반응식
[CH2:1]1[C:10]2[CH:9]=[CH:8][CH:7]=[C:6]([C:11](Cl)=[O:12])[C:5]=2[CH2:4][CH2:3][CH2:2]1.[Cl:14][C:15]1[CH:16]=[C:17]([C@@H:22]([CH2:26][N:27]2[CH:31]=[CH:30][N:29]=[CH:28]2)[CH2:23][CH2:24][OH:25])[CH:18]=[CH:19][C:20]=1[Cl:21].C(N([CH2:37][CH3:38])CC)C>C(#N)C>[CH2:1]1[C:10]2[CH:9]=[CH:8][CH:7]=[C:6]([C:11]([O:25][CH2:24][CH2:23][C@@H:22]([C:17]3[CH:18]=[CH:19][C:20]([Cl:21])=[C:15]([Cl:14])[CH:16]=3)[CH2:26][N:27]3[CH:31]=[CH:30][N:29]=[C:28]3[C:11]([C:6]3[C:5]4[CH2:4][CH2:3][CH2:2][CH2:1][C:10]=4[CH:9]=[CH:37][CH:38]=3)=[O:12])=[O:12])[C:5]=2[CH2:4][CH2:3][CH2:2]1

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 27531625,6,7,8-Tetrahydronaphthalene-1-carbonyl chlorideHCID 541546783(S)-(3,4-dichlorophenyl)-4-(imidazol-1-yl)butan-1-ol

생성물 1

HCID 598865763(S)-(3,4-dichlorophenyl)-4-[2-(1,2,3,4-tetrahydro-5-naphthoyl)imidazol-1-yl]butyl 1,2,3,4-tetrahydro-5-naphthoate수율 72.7%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

1,2,3,4-Tetrahydro-5-naphthoyl chloride (1.70 g) (see Preparation 36) was added dropwise to a suspension of 3(S)-(3,4-dichlorophenyl)-4-(imidazol-1-yl)butan-1-ol (0.90 g) (see Preparation 99) and triethylamine (1.45 g) in anhydrous acetonitrile (15 ml) and the solution stirred at room temperature for 4 days. The solvent was then removed under reduced pressure to give a residue which was partitioned between ethyl acetate and saturated aqueous sodium hydrogen carbonate solution. The phases were separated and the aqueous phase further extracted with ethyl acetate. The organic phases were combined, washed sequentially with water and brine, dried over anhydrous sodium sulphate and the solvent removed under reduced pressure to give a residue which was chromatographed on silica gel eluting with a solvent gradient of 2:1 changing to 0:1, by volume, pentane:ethyl acetate to give 3(S)-(3,4-dichlorophenyl)-4-[2-(1,2,3,4-tetrahydro-5-naphthoyl)imidazol-1-yl]butyl 1,2,3,4-tetrahydro-5-naphthoate (1.38 g) as a gum.

후처리

  1. customThe solvent was then removed under reduced pressure
  2. customto give a residue which
  3. customwas partitioned between ethyl acetate and saturated aqueous sodium hydrogen carbonate solution
  4. customThe phases were separated
  5. extractionthe aqueous phase further extracted with ethyl acetate
  6. washwashed sequentially with water and brine
  7. dry with materialdried over anhydrous sodium sulphate
  8. customthe solvent removed under reduced pressure
  9. customto give a residue which
  10. customwas chromatographed on silica gel eluting with a solvent gradient of 2:1 changing to 0:1, by volume, pentane

출처 및 근거

ORD 기록
ord-f226241f207e442a87ef41ed801b089d
출처 데이터셋
uspto-grants-2001_03
특허 번호
US06207678B1

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