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Cesium fluoride → Ethyl 2-(4-amino-2-chloro-5-ethynylphenoxy)-4-fluorobenzoate

HRID 1848864
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인쇄 미리보기

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HRID 1848864 반응식
[NH2:1][C:2]1[C:20]([C:21]#[C:22][Si](C)(C)C)=[CH:19][C:5]([O:6][C:7]2[CH:17]=[C:16]([F:18])[CH:15]=[CH:14][C:8]=2[C:9]([O:11][CH2:12][CH3:13])=[O:10])=[C:4]([Cl:27])[CH:3]=1.[F-].[Cs+]>CO>[NH2:1][C:2]1[C:20]([C:21]#[CH:22])=[CH:19][C:5]([O:6][C:7]2[CH:17]=[C:16]([F:18])[CH:15]=[CH:14][C:8]=2[C:9]([O:11][CH2:12][CH3:13])=[O:10])=[C:4]([Cl:27])[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 25953Cesium fluorideHCID 67226491Ethyl 2-(4-amino-2-chloro-5-((trimethylsilyl)ethynyl)phenoxy)-4-fluorobenzoate

생성물 1

HCID 87316240Ethyl 2-(4-amino-2-chloro-5-ethynylphenoxy)-4-fluorobenzoate

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of EXAMPLE 242C (2.69 g) in methanol (20 mL) was added CsF (5 g). The mixture was stirred at room temperature overnight. The solvent was evaporated and the residue was dissolved in ethyl acetate (200 mL) and washed with water, brine and dried over Na2SO4. The mixture was filtered, and the solvent was evaporated.

후처리

  1. customThe solvent was evaporated
  2. dissolutionthe residue was dissolved in ethyl acetate (200 mL)
  3. washwashed with water, brine
  4. dry with materialdried over Na2SO4
  5. filtrationThe mixture was filtered
  6. customthe solvent was evaporated

출처 및 근거

ORD 기록
ord-f6b0cbd5cba84ac29a09928d665d97bb
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08952157B2

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