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Ammonia → 5,6,7,8-Tetrahydro-2-phenyl-3-(benzoylaminoiminomethyl)imidazo[2,1-b]benzothiazole

HRID 580926
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HRID 580926 반응식
[C:1]1([C:7]2[N:8]=[C:9]3[N:13]([C:14]=2[CH:15]=O)[C:12]2[CH2:17][CH2:18][CH2:19][CH2:20][C:11]=2[S:10]3)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:21]([NH:29][NH2:30])(=[O:28])[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1.Cl.C(O)C.N>O>[C:1]1([C:7]2[N:8]=[C:9]3[N:13]([C:14]=2[CH:15]=[N:30][NH:29][C:21](=[O:28])[C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[C:12]2[CH2:17][CH2:18][CH2:19][CH2:20][C:11]=2[S:10]3)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 222AmmoniaHCID 11955BenzoylhydrazineHCID 107316142-Phenyl-4,5,6,7,8-pentahydroimidazo[2,1-b]benzothiazole-3-carbaldehydeHCID 21887872Ethanol hydrochloride

생성물 1

HCID 23145105,6,7,8-Tetrahydro-2-phenyl-3-(benzoylaminoiminomethyl)imidazo[2,1-b]benzothiazole수율 84%

시약·촉매·용매 1

HCID 962
Water
용매

실험 절차

0.28 g of 5,6,7,8-tetrahydro-2-phenyl-3-formylimidazo[2,1-b]benzothiazole and 0.15 g of benzohydrazide were stirred over night in 20 ml of a 0.1N hydrochloric acid-ethanol solution at room temperature and the precipitated crystal obtained by filtration. The crystals were dissolved in water and the solution was made alkaline by ammonia solution, then extracted by chloroform. The extract was washed with water and dried, then the solvent was distilled off and the residue was crystallized from ethyl acetate to obtain the desired substance in an amount of 0.35 g (yield of 84.0%).

후처리

  1. customthe precipitated crystal obtained by filtration
  2. extractionextracted by chloroform
  3. washThe extract was washed with water
  4. customdried
  5. distillationthe solvent was distilled off
  6. customthe residue was crystallized from ethyl acetate
  7. customto obtain the desired substance in an amount of 0.35 g (yield of 84.0%)

출처 및 근거

ORD 기록
ord-6b09b8036967419295bf960b4f73ea62
출처 데이터셋
uspto-grants-1999_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05919799

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