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Lithium diisopropylamide → 3-(4-Bromo-2-chloro-benzyl)-1-(4,4-difluoro-cyclohexyl)-pyrrolidin-2-one

HRID 1672742
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HRID 1672742 반응식
[F:1][C:2]1([F:14])[CH2:7][CH2:6][CH:5]([N:8]2[CH2:12][CH2:11][CH2:10][C:9]2=[O:13])[CH2:4][CH2:3]1.[Li+].CC([N-]C(C)C)C.[Br:23][C:24]1[CH:29]=[CH:28][C:27]([CH2:30]Br)=[C:26]([Cl:32])[CH:25]=1>C1COCC1.CCCCCC>[Br:23][C:24]1[CH:29]=[CH:28][C:27]([CH2:30][CH:10]2[CH2:11][CH2:12][N:8]([CH:5]3[CH2:4][CH2:3][C:2]([F:1])([F:14])[CH2:7][CH2:6]3)[C:9]2=[O:13])=[C:26]([Cl:32])[CH:25]=1
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참가 물질

6

반응물 3

HCID 2724682Lithium diisopropylamideHCID 219144864-Bromo-1-(bromomethyl)-2-chlorobenzeneHCID 57878591HCID 57878591, 화합물

생성물 1

HCID 578786043-(4-Bromo-2-chloro-benzyl)-1-(4,4-difluoro-cyclohexyl)-pyrrolidin-2-one

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매HCID 8058
Hexane
용매

실험 절차

To a solution of 1-(4,4-difluoro-cyclohexyl)-pyrrolidin-2-one (190 mg, 0.94 mmol) in 10 mL dry THF, add 1.04 mL of 1.5M LDA (1.5 eq.) in hexane dropwise at −78° C. Then, add 0.59 g of 4-bromo-1-bromomethyl-2-chloro-benzene (1.5 eq) at −78° C. Allow the resulting solution to stand at room temp for overnight. Quench the mixture with saturated aqueous NaCl and extract with Et2O. Wash the organic layer with water, then brine, and dry over Na2SO4, filter and concentrate. Purify the crude material by chromatography to afford the title compound: mass spectrum (m/z): 407 (M+1).

후처리

  1. customQuench the mixture with saturated aqueous NaCl
  2. extractionextract with Et2O
  3. washWash the organic layer with water
  4. dry with materialbrine, and dry over Na2SO4
  5. filtrationfilter
  6. concentrationconcentrate
  7. customPurify the crude material by chromatography

출처 및 근거

ORD 기록
ord-11eb263ef19c4f67b46367a0fa0016c0
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07998999B2

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