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Ammonia → benzyl N-(2-sulfamoylethyl)carbamate

HRID 1405941
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HRID 1405941 반응식
[NH3:1].O1CCOCC1.[CH2:8]([O:15][C:16]([NH:18][CH2:19][CH2:20][S:21](Cl)(=[O:23])=[O:22])=[O:17])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1>C(#N)C>[CH2:8]([O:15][C:16]([NH:18][CH2:19][CH2:20][S:21]([NH2:1])(=[O:23])=[O:22])=[O:17])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 222AmmoniaHCID 312751,4-DioxaneHCID 13255033Benzyl [2-(chlorosulfonyl)ethyl]carbamate

생성물 1

HCID 11615848benzyl N-(2-sulfamoylethyl)carbamate수율 74%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

In a reaction flask, 100 ml of aqueous ammonia and 100 ml of dioxane were added, and a solution of 17.9 g 2-benzyloxyformamidoethylsulfonyl chloride in acetonitrile (30 ml) was added dropwise under ice-bath condition. The mixture was stirred for 2 h at room temperature. Upon the end of the dropping, the mixture was concentrated under a reduced pressure, and was then filtered, the filter cake was washed with water, and dried to obtain 12.3 g of white solid, yield 74%.

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후처리

  1. concentrationUpon the end of the dropping, the mixture was concentrated under a reduced pressure
  2. filtrationwas then filtered
  3. washthe filter cake was washed with water
  4. customdried

출처 및 근거

ORD 기록
ord-2e84be28666b4e1282446e0f9bb9ae8f
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08916574B2

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