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Ethyl Acetate → HCID 86739105, 화합물

HRID 1648795
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HRID 1648795 반응식
[CH:1]([N:4](SSN(C(C)C)S(C1C=CC(C)=CC=1)(=O)=O)[S:5](C1C=CC(C)=CC=1)(=O)=O)(C)C.ClCl.[S:33](Cl)(Cl)(=[O:35])=[O:34].CN[CH:40]=[N:41][C:42]1[CH:47]=[CH:46][C:45]([CH3:48])=[CH:44][C:43]=1[CH3:49].CNC=[N:53][C:54]1[CH:59]=[C:58](Cl)[CH:57]=[CH:56][C:55]=1C.[C:62](OCC)(=O)C>>[C:42]1([N:41]=[CH:40][CH2:1][NH:4][S:5][N:53]([C:54]2[CH:55]=[CH:56][CH:57]=[CH:58][CH:59]=2)[S:33]([CH3:62])(=[O:35])=[O:34])[CH:47]=[CH:46][C:45]([CH3:48])=[CH:44][C:43]=1[CH3:49]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 6

HCID 8857Ethyl AcetateHCID 24526ChlorineHCID 24648Sulfuryl chlorideHCID 20481811HCID 20481811, 화합물HCID 178484910HCID 178484910, 화합물HCID 178484923HCID 178484923, 화합물

생성물 1

HCID 86739105HCID 86739105, 화합물
수율 14%

실험 절차

Following the procedure for Example 2, but substituting N,N'-dithiobis[N-pheylmethanesulfonamide] for N,N'-dithiobis-[N-isopropyl-p-toluenesulfonamide], chlorine for sulfuryl chloride, and N-methyl-N'-2,4-xylylformamidine for N-methyl-N'-(4-chloro-o-tolyl) formamidine, the product is prepared. The product is recrytallized from ethyl acetate to give 2.0 g. (14% yield) of N-[[[N-2,4-xylylformimidoyl]methylamino]thio]-N-phenylmethanesulfonamide as white crystals, mp. 120°-121.5°.

후처리

  1. customthe product is prepared
  2. customto give 2.0 g

출처 및 근거

ORD 기록
ord-07d2941ceb6a4c18abc986f46e81cbbd
출처 데이터셋
uspto-grants-1983_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04413013

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