Methyl iodide → 3-methylthio-2H-1,4-benzothiazine

HRID 27743ノート

反応式

HRID 27743 の反応式
[H-].[Na+].[S:3]1[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[NH:6][C:5](=[S:13])[CH2:4]1.I[CH3:15]>O1CCCC1>[CH3:15][S:13][C:5]1[CH2:4][S:3][C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[N:6]=1

参加物

5

反応物 3

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 7739812H-1,4-Benzothiazine-3(4H)-thione

生成物 1

HCID 125454293-methylthio-2H-1,4-benzothiazine

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To 17 parts of sodium hydride in 1500 parts of tetrahydrofuran at room temperature under nitrogen is added, portionwise with stirring during approximately 15 minutes, 90 parts of 2H-1,4-benzothiazine-3(4H)-thione [J. Med. Chem. 12, 290 (1969)]. After the addition is complete, stirring under nitrogen is continued for 10 minutes, whereupon a solution of 85 parts of iodomethane in 70 parts of tetrahydrofuran is rapidly stirred in and stirring continued thereafter for a still further 15 minutes. Removal of solvent by vacuum distillation under nitrogen affords 3-methylthio-2H-1,4-benzothiazine as the residue. Since the product is subject to spontaneous hydrolytic decomposition, it is not usually isolated for the purposes of this invention but instead is employed as the solution in tetrahydrofuran preparable via the foregoing procedure.

後処理

  1. additionAfter the addition
  2. stirringstirring under nitrogen
  3. stirringis rapidly stirred in and
  4. stirringstirring
  5. waitfor a still further 15 minutes
  6. customRemoval of solvent
  7. distillationby vacuum distillation under nitrogen

出典と根拠

ORDレコード
ord-177eee20f9c144d989d36dc5c1aa107e
出典データセット
uspto-grants-1980_09
特許番号
US04223136

反応ノート

読み込み中…