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Hydrochloric Acid → Octahydropyrazino[2,1-c][1,4]thiazine 2,2-dioxide

HRID 2074835
ノート
印刷プレビュー

反応式

HRID 2074835 の反応式
[CH2:1]1[CH:6]2[C:7](=O)[NH:8][CH2:9][CH2:10][N:5]2[CH2:4][CH2:3][S:2]1(=[O:13])=[O:12].Cl>C1COCC1>[CH2:1]1[CH:6]2[CH2:7][NH:8][CH2:9][CH2:10][N:5]2[CH2:4][CH2:3][S:2]1(=[O:13])=[O:12]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 313Hydrochloric AcidHCID 59215885Hexahydropyrazino[2,1-c][1,4]thiazin-9(6H)-one 2,2-dioxide

生成物 1

HCID 59215787Octahydropyrazino[2,1-c][1,4]thiazine 2,2-dioxide収率 111.6%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
50 °C

実験手順

To a suspension of hexahydropyrazino[2,1-c][1,4]thiazin-9(6H)-one 2,2-dioxide (D18; 165 mg, 0.81 mmol) in 1 ml of anhydrous THF were added successive aliquots of a 1M solution of borane THF complex in THF (total 20.4 ml, 20.4 mmol) and the reaction stirred at room temperature and 50° C., until disappearance of the starting material. Hydrochloric acid (5M, 2 ml) was added to the solution and stirring was continued at 50° C. for 12 h. The solvent was removed under reduced pressure and the residue loaded on a SCX cartridge, washed with methanol and eluted with 0.5M methanolic ammonia. The basic fractions were collected and the solvent removed leaving 172 mg of the target product, partially contaminated by the starting material.

後処理

  1. stirringstirring
  2. customThe solvent was removed under reduced pressure
  3. washwashed with methanol
  4. washeluted with 0.5M methanolic ammonia
  5. customThe basic fractions were collected
  6. customthe solvent removed

出典と根拠

ORDレコード
ord-34cfe6bec5144f36be3e34c319e9f856
出典データセット
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07919491B2

反応ノート

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