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4-Toluenesulfonyl chloride → HCID 86739786, 화합물

HRID 1153965
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HRID 1153965 반응식
OCCC[N:5]1C(=O)N(CCOC2C=CC=CC=2)C(CC)=[N:6]1.[S:22]([C:26]1[CH:32]=[CH:31][C:29]([CH3:30])=[CH:28][CH:27]=1)([O-:25])(=[O:24])=[O:23].C([N:35](CC)[CH2:36][CH3:37])C.S(Cl)(C1C=CC(C)=CC=1)(=O)=[O:41]>C(Cl)Cl.CN(C1C=CN=CC=1)C.O>[S:22]([C:26]1[CH:32]=[CH:31][C:29]([CH3:30])=[CH:28][CH:27]=1)([OH:25])(=[O:24])=[O:23].[N:35]1[N:5]=[N:6][C:37](=[O:41])[CH:36]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 73974-Toluenesulfonyl chlorideHCID 8471TriethylamineHCID 85570p-ToluenesulfonateHCID 10379527HCID 10379527, 화합물

생성물 1

HCID 86739786HCID 86739786, 화합물

시약·촉매·용매 3

HCID 142844-(Dimethylamino)pyridine촉매
HCID 962
Water
용매
HCID 6344Dichloromethane용매

실험 절차

The alcohol is converted to the tosylate by dissolving in methylene chloride containing N,N-dimethyl-4-aminopyridine (0.05 mol eq) and triethylamine (1.05 mol eq) and treating with tosyl chloride (1.1 mole eq) added in one portion at 0° C. with stirring. After standing for about 24 hr. at 0° C., the mixture is treated with water and extracted several times with methylene chloride. The combined methylene chloride extracts are dried over magnesium sulfate, filtered and concentrated under reduced pressure. Flash chromatography of residual material affords 2-[3-(p-toluenesulfonate)propyl]-5-ethyl-2,4-dihydro-4-(2-phenoxyethyl)-3H-1,2,4-triazol-3-one (XV, Y=H, X1 =0, n=2, R2 =C2H5).

후처리

  1. additionadded in one portion at 0° C.
  2. extractionextracted several times with methylene chloride
  3. dry with materialThe combined methylene chloride extracts are dried over magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-ca12cd3df928430db815c350cc4a9720
출처 데이터셋
uspto-grants-1984_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04487773

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