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Ammonia → 3-(1,1-Dimethylethylsulfinamido)oxetane-3-carboximidamide

HRID 1892558
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HRID 1892558 반응식
[C:1]([C:3]1([NH:7][S:8]([C:10]([CH3:13])([CH3:12])[CH3:11])=[O:9])[CH2:6][O:5][CH2:4]1)#[N:2].C([NH:17][C@H](C(O)=O)CS)(=O)C.N>CO>[CH3:11][C:10]([CH3:13])([S:8]([NH:7][C:3]1([C:1](=[NH:17])[NH2:2])[CH2:4][O:5][CH2:6]1)=[O:9])[CH3:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 222AmmoniaHCID 12035N-Acetyl-L-CysteineHCID 67957830N-(3-cyanooxetan-3-yl)-2-methylpropane-2-sulfinamide

생성물 1

HCID 679578843-(1,1-Dimethylethylsulfinamido)oxetane-3-carboximidamide

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

To a mixture of N-(3-cyanooxetan-3-yl)-2-methylpropane-2-sulfinamide (0.1 g, 0.494 mmol) in methanol (2 ml) in a 50 ml sealed tube was added N-acetyl-L-(+)-cysteine (0.081 g, 0.494 mmol), and the reaction mixture stirred for few minutes. A solution of ammonia in methanol (0.5 ml, 3.50 mmol, 7 N) was added, and the reaction mixture stirred at 60° C. for overnight. The reaction mixture was then concentrated under vacuum, and the crude was used for the next step without further purification.

후처리

  1. customsealed tube
  2. stirringthe reaction mixture stirred at 60° C. for overnight
  3. concentrationThe reaction mixture was then concentrated under vacuum
  4. customthe crude was used for the next step without further purification

출처 및 근거

ORD 기록
ord-389ccd3d7dcf458e8eba9b9d99eab6d4
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08507683B2

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