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Sodium Iodide → N-{[7-(Methylsulfonyl)-4H-1,3-benzodioxin-2-YL]methyl}propan-2-amine

HRID 452397
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HRID 452397 반응식
Cl[CH2:2][CH:3]1[O:8][C:7]2[CH:9]=[C:10]([S:13]([CH3:16])(=[O:15])=[O:14])[CH:11]=[CH:12][C:6]=2[CH2:5][O:4]1.[CH3:17][CH:18]([NH2:20])[CH3:19].C(=O)([O-])[O-].[K+].[K+].[I-].[Na+]>C(#N)C>[CH3:16][S:13]([C:10]1[CH:11]=[CH:12][C:6]2[CH2:5][O:4][CH:3]([CH2:2][NH:20][CH:18]([CH3:19])[CH3:17])[O:8][C:7]=2[CH:9]=1)(=[O:15])=[O:14]
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참가 물질

6

반응물 4

HCID 5238Sodium IodideHCID 6363IsopropylamineHCID 11430Potassium CarbonateHCID 668873282-(chloromethyl)-7-(methylsulfonyl)-4H-1,3-benzodioxine

생성물 1

HCID 44481358N-{[7-(Methylsulfonyl)-4H-1,3-benzodioxin-2-YL]methyl}propan-2-amine수율 56.3%

시약·촉매·용매 1

HCID 6342
Acetonitrile
용매

실험 절차

A mixture of 2-(chloromethyl)-7-(methylsulfonyl)-4H-1,3-benzodioxine (0.1 g, 0.38 mmol), propan-2-amine (1.30 ml, 152 mmol), potassium carbonate (80 mg, 0.57 mmol), some few crystals of sodium iodide in ACN (3 ml) was heated in a micro wave oven at 170° C. for 40 min. After cooling to ambient temperature the volatiles were evaporated in vacuum. The oily residue was chromatographed twice on a silica column with EtOAc/MeOH (7:1) as eluent. Collection of the fractions containing pure product and evaporation of the solvent afforded the title compound (61 mg, 55%). MS m/z (rel. intensity, 70 eV) 285 (M+, 1), 123 (11), 86 (15), 77 (16), 72 (bp).

후처리

  1. customwere evaporated in vacuum
  2. customThe oily residue was chromatographed twice on a silica column with EtOAc/MeOH (7:1) as eluent
  3. customCollection of the fractions
  4. additioncontaining pure
  5. customproduct and evaporation of the solvent

출처 및 근거

ORD 기록
ord-572d120304614b96b18f338366d6326a
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08492372B2

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