4-Methylmorpholine → HCID 178502897, 화합물

HRID 1584032노트

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HRID 1584032 반응식
[SH:1][C:2]1[N:6]([CH2:7][C:8]([OH:10])=O)[N:5]=[N:4][N:3]=1.CN1CCOCC1.ClC(OCC)=O.Cl.[CH3:25][O:26][NH2:27]>O1CCCC1>[CH3:25][O:26][NH:27][C:8](=[O:10])[CH2:7][N:6]1[C:2]([SH:1])=[N:3][N:4]=[N:5]1

참가 물질

6

실험 절차

To a solution cooled at -28° C. to -35° C. of 5-mercapto-1H-tetrazole-1-acetic acid (0.8 g) in tetrahydrofuran (40 ml) are added N-methylmorpholine (1.26 ml) and ethyl chloroformate (0.62 ml). After stirring for 1 hour, a solution of methoxyamine hydrochloride (0.34 g) and N-methylmorpholine (0.71 ml) in tetrahydrofuran (11 ml) is added to the mixture at -50° C. After 2 hours' stirring at about -30° C., the mixture is concentrated under reduced pressure, and the resultant mixture is diluted with water (50 ml) and ethyl acetate (50 ml). The mixture is acidified to pH 2 with hydrochloric acid and extracted with ethyl acetate. The extract solution is dried over magnesium sulfate and concentrated to give 5-mercapto-1H-tetrazole-1-acetohydroxamic acid methyl ester. mp. 165°-167° C. (decomp.).

후처리

  1. stirringAfter 2 hours' stirring at about -30° C.
  2. concentrationthe mixture is concentrated under reduced pressure
  3. additionthe resultant mixture is diluted with water (50 ml) and ethyl acetate (50 ml)
  4. extractionextracted with ethyl acetate
  5. dry with materialThe extract solution is dried over magnesium sulfate
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-3a34622dbf2a435b8dd1bcae3112c30e
출처 데이터셋
uspto-grants-1985_11
특허 번호
US04555578

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