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Sodium Acetate → 2-Amino-5-methyl-4,5,6-trihydrobenzothiazol-7-one

HRID 879256
ノート
印刷プレビュー

反応式

HRID 879256 の反応式
Br[CH:2]1[C:7](=[O:8])[CH2:6][CH:5]([CH3:9])[CH2:4][C:3]1=O.C([O-])(=O)C.[Na+].[NH2:16][C:17]([NH2:19])=[S:18]>C(O)(=O)C>[NH2:19][C:17]1[S:18][C:2]2[C:7](=[O:8])[CH2:6][CH:5]([CH3:9])[CH2:4][C:3]=2[N:16]=1
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

5

反応物 3

HCID 517045Sodium AcetateHCID 2723790ThioureaHCID 669327192-Bromo-5-methylcyclohexane-1,3-dione

生成物 1

HCID 27565102-Amino-5-methyl-4,5,6-trihydrobenzothiazol-7-one

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

反応条件

温度
100 °C

実験手順

To a solution of 24 in acetic acid (540 mL) was added sodium acetate (44.3 g, 540 mmol) and thiourea (28.8 g, 378 mmol). The reaction mixture was stirred with a mechanical stirrer at 100° C. for 3 h. The reaction mixture was partially concentrated in vacuo. EtOAc was added (500 mL). The mixture was made basic with 1 M NaOH, and the layers were separated. The aqueous layer was extracted with EtOAc (2×300 mL). The combined organic layers were dried, filtered, and concentrated in vacuo to give 49.3 g of 25, which was taken on without further purification. LCMS-ESI+: calc'd for C8H11N2OS: 183.1 (M+H+); Found: 183.1 (M+H+).

後処理

  1. concentrationThe reaction mixture was partially concentrated in vacuo
  2. additionEtOAc was added (500 mL)
  3. customthe layers were separated
  4. extractionThe aqueous layer was extracted with EtOAc (2×300 mL)
  5. customThe combined organic layers were dried
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-928c7de9f3c6416ab9a1e10bfda5660e
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08987250B2

反応ノート

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