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Sulfamide → HCID 58244794, 화합물

HRID 1408312
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HRID 1408312 반응식
[CH3:1][NH:2][CH2:3][CH2:4][CH2:5][CH2:6][NH:7][C:8](=[O:14])[O:9][C:10]([CH3:13])([CH3:12])[CH3:11].[S:15](=[O:19])(=[O:18])(N)[NH2:16]>O1CCOCC1.C(OC(C)C)(C)C>[C:10]([O:9][C:8](=[O:14])[NH:7][CH2:6][CH2:5][CH2:4][CH2:3][N:2]([S:15]([NH2:16])(=[O:19])=[O:18])[CH3:1])([CH3:11])([CH3:13])[CH3:12]
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참가 물질

5

반응물 2

HCID 82267SulfamideHCID 20709354tert-Butyl [4-(methylamino)butyl]carbamate

생성물 1

HCID 58244794HCID 58244794, 화합물수율 64%

시약·촉매·용매 2

HCID 7914Diisopropyl Ether용매HCID 312751,4-Dioxane용매

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온도
100 °C

실험 절차

A mixture of tert-butyl 4-(methylamino)butylcarbamate (4 g, 19.77 mmoles) and sulfuric diamide (7.6 g, 4 eq) in dioxane (10 mL) was heated at 100° C. in a microwave oven during 30 minutes. The RM was then concentrated in vacuo, and DCM was added. The resulting white precipitate of sulfuric diamide in excess was filtered off, and the filtrate was successively washed with diluted HCl, then brine, dried over magnesium sulfate, filtered and concentrated. Trituration in diisopropyl ether afforded 3.55 g (64% yield) of tert-butyl 4-(methyl(sulfamoyl)amino)butylcarbamate 10b as a white solid; m/z 282 [M+H]+.

후처리

  1. concentrationThe RM was then concentrated in vacuo, and DCM
  2. additionwas added
  3. filtrationThe resulting white precipitate of sulfuric diamide in excess was filtered off
  4. washthe filtrate was successively washed with diluted HCl
  5. dry with materialbrine, dried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-538cf01c411f44fea189861f0f5b33a6
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08921355B2

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