Lithium Chloride → HCID 89996171, 화합물

HRID 2276045노트

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HRID 2276045 반응식
[Cl:1][C:2]1[N:7]=[C:6]([CH2:8][Cl:9])[C:5](I)=[CH:4][CH:3]=1.C([Mg]Cl)(C)C.[Li+].[Cl-].[C:18]([N:25]1[CH2:28][C:27](=[O:29])[CH2:26]1)([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19]>C1COCC1>[C:21]([O:20][C:18]([N:25]1[CH2:28][C:27]([C:5]2[C:6]([CH2:8][Cl:9])=[N:7][C:2]([Cl:1])=[CH:3][CH:4]=2)([OH:29])[CH2:26]1)=[O:19])([CH3:24])([CH3:22])[CH3:23]

참가 물질

6

실험 절차

To a stirred solution of 6-chloro-2-chloromethyl-3-iodo-pyridine (2.5 g, 8.7 mmol, 1 eq) in dry THF (25 mL) was added i-PrMgCl.LiCl complex (1.3M in THF, 7.37 mL, 9.6 mmol, 1.1 eq) at −20° C. in drop wise manner over period of 10 minutes. Pre-dissolved solution of N-boc-3-azetidinone (1.78 g, 10.4 mmol, 1.2 eq) in dry THF (10 mL) was added at −20° C. to above reaction mixture. Resulting reaction mixture was stirred at room temperature for 16 hours under nitrogen atmosphere. After maximum consumption of starting material, reaction mixture was cooled to 0° C., quenched with 10% citric acid solution (20 mL) and extracted with ethyl acetate (3×100 mL). Combined organic phase was dried over anhydrous Na2SO4 and concentrated under reduced pressure to get brown oil (4.5 g, crude). Crude of title compound was used as such for next reaction. LC-MS (m/z): 332.9 (M+H).

후처리

  1. customResulting
  2. customreaction mixture
  3. customAfter maximum consumption of starting material, reaction mixture
  4. temperaturewas cooled to 0° C.
  5. customquenched with 10% citric acid solution (20 mL)
  6. extractionextracted with ethyl acetate (3×100 mL)
  7. dry with materialCombined organic phase was dried over anhydrous Na2SO4
  8. concentrationconcentrated under reduced pressure
  9. customto get brown oil (4.5 g, crude)

출처 및 근거

ORD 기록
ord-0954f20113da420d9c1d6887171b8abd
출처 데이터셋
uspto-grants-2015_09
특허 번호
US09131697B2

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