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Sodium Iodide → HCID 86668046, 화합물

HRID 474075
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HRID 474075 반응식
[Br:1][C:2]1[CH:7]=[C:6]([C:8]([NH:13][C:14](=[O:17])[CH2:15]Cl)([CH2:11][OH:12])[CH2:9][OH:10])[CH:5]=[CH:4][N:3]=1.CC([O-])(C)C.[K+].[Na+].[I-]>CC(O)(C)C>[Br:1][C:2]1[CH:7]=[C:6]([C:8]2([CH2:11][OH:12])[NH:13][C:14](=[O:17])[CH2:15][O:10][CH2:9]2)[CH:5]=[CH:4][N:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 5238Sodium IodideHCID 23665647Potassium tert-butoxideHCID 86668045HCID 86668045, 화합물

생성물 1

HCID 86668046HCID 86668046, 화합물

시약·촉매·용매 1

HCID 6386tert-Butanol용매

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온도
90 °C

실험 절차

To a solution of N-[1-(2-bromo-pyridin-4-yl)-2-hydroxy-1-hydroxymethyl-ethyl]-2-chloro-acetamide (8.0 g, 24.8 mmol) in t-BuOH (50 ml) was added t-BuOK (5.5 g, 49.6 mmol) and NaI (0.375 g, 2.48 mmol) and heated to 90° C. for 1 h. Reaction mass was concentrated under reduced pressure and diluted the residue with EtOAc. Organic layer was separated and washed with ammonium chloride solution, brine followed by drying over anhy. Na2SO4. The crude product was purified by column chromatography using 5% methanol in DCM to obtain title compound as a pale brown gum. Yield=3.25 g (46%). TLC (ethyl acetate) Rf=0.17; LCMS: RtH8=0.12; [M+1]+=286.7 and 289.

후처리

  1. customReaction mass
  2. concentrationwas concentrated under reduced pressure
  3. additiondiluted the residue with EtOAc
  4. customOrganic layer was separated
  5. washwashed with ammonium chloride solution, brine
  6. customby drying over anhy
  7. customThe crude product was purified by column chromatography

출처 및 근거

ORD 기록
ord-86e71ccae45d433a8ceab5edcfba2ce0
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08637508B2

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