4-Methylmorpholine → HCID 178502897、化合物

HRID 1584032ノート

反応式

HRID 1584032 の反応式
[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

参加物

6

実験手順

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.).

後処理

  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

出典と根拠

ORDレコード
ord-3a34622dbf2a435b8dd1bcae3112c30e
出典データセット
uspto-grants-1985_11
特許番号
US04555578

反応ノート

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