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Sodium Iodide → N-Methoxy-N-methyl-3-morpholin-4-yl-5-(pentafluorosulfanyl)benzamide

HRID 532390
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HRID 532390 반응식
[NH2:1][C:2]1[CH:3]=[C:4]([CH:11]=[C:12]([S:14]([F:19])([F:18])([F:17])([F:16])[F:15])[CH:13]=1)[C:5]([N:7]([O:9][CH3:10])[CH3:8])=[O:6].C(=O)([O-])[O-].[Cs+].[Cs+].[I-].[Na+].Br[CH2:29][CH2:30][O:31][CH2:32][CH2:33]Br>CN(C=O)C.CC(=O)OCC>[CH3:10][O:9][N:7]([CH3:8])[C:5](=[O:6])[C:4]1[CH:11]=[C:12]([S:14]([F:19])([F:15])([F:16])([F:17])[F:18])[CH:13]=[C:2]([N:1]2[CH2:33][CH2:32][O:31][CH2:30][CH2:29]2)[CH:3]=1
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참가 물질

7

반응물 4

HCID 5238Sodium IodideHCID 10796Cesium carbonateHCID 21521Bis(2-bromoethyl) etherHCID 580857033-Amino-N-methoxy-N-methyl-5-pentafluorosulfanylbenzamide

생성물 1

HCID 58136881N-Methoxy-N-methyl-3-morpholin-4-yl-5-(pentafluorosulfanyl)benzamide수율 32%

시약·촉매·용매 2

HCID 6228
Dimethylformamide
용매
HCID 8857Ethyl Acetate용매

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온도
130 °C

실험 절차

3-Amino-N-methoxy-N-methyl-5-(pentafluorosulfanyl)benzamide (O5.075; 6.3 g) was dissolved in DMF (80 ml), and cesium carbonate (10.1 g), sodium iodide (0.62 g) and bis(2-bromoethyl)ether (19.37 g) were added. The mixture was divided between 10 microwave vessels, each of which was heated to 130° C. for 3 h. Subsequently, the batches were combined and freed of solvent. The residue was taken up in EA and washed with water. The EA phase was dried and concentrated. The residue was purified using silica gel (120 g cartridge, n-heptane/EA gradient of 0-100% within 30 min). 2.48 g of the title compound were obtained.

후처리

  1. washwashed with water
  2. dry with materialThe EA phase was dried
  3. concentrationconcentrated
  4. customThe residue was purified
  5. customsilica gel (120 g cartridge, n-heptane/EA gradient of 0-100% within 30 min)

출처 및 근거

ORD 기록
ord-b0eb5626dc754def928e1e88ac969627
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08853206B2

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