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Hydrochloric Acid → HCID 66759651、化合物

HRID 389479
ノート
印刷プレビュー

反応式

HRID 389479 の反応式
[Br:1][C:2]1[C:10]2[S:9][CH:8]=[N:7][C:6]=2[CH:5]=[CH:4][C:3]=1N.Cl.N([O-])=O.[Na+].[I-:17].[K+].S([O-])([O-])(=O)=S.[Na+].[Na+]>O>[Br:1][C:2]1[C:10]2[S:9][CH:8]=[N:7][C:6]=2[CH:5]=[CH:4][C:3]=1[I:17]
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

7

反応物 5

HCID 313Hydrochloric AcidHCID 4875Potassium IodideHCID 24477Sodium ThiosulfateHCID 47126206-Amino-7-bromobenzothiazoleHCID 23668193Sodium Nitrite

生成物 1

HCID 66759651HCID 66759651、化合物収率 5%

試薬・触媒・溶媒 1

HCID 962
Water
溶媒
4 回

反応条件

温度
0 °C

実験手順

To a suspension of 7-bromo-benzothiazol-6-ylamine (7.6 g, 33.3 mmol) in water (60 mL) was added concentrated hydrochloric acid (6 mL, 72 mmol). The mixture was cooled to 0° C. and stirred for 10 min. A cooled (0° C.) solution of sodium nitrite (5.0 g, 73 mmol) in water (10 mL) was added dropwise to the reaction mixture keeping the internal temperature below 5° C. The mixture was stirred for further 10 min. A solution of potassium iodide (12.1 g, 73 mmol) in water (15 mL) was added to the reaction mixture and was stirred vigorously for 10 min, and then water (200 mL) and 20% aqueous sodium thiosulfate solution (100 mL) were added. The solid formed was extracted with ethyl acetate (3×70 mL). The combined organic fractions were washed with water (100 mL), dried over anhydrous sodium sulfate, and concentrated. Purification of the residue by column chromatography (25% ethyl acetate:hexanes) afforded 0.3 g (5%) of the title compound, plus some impure title compound. The impure title compound was recrystallized 2× from 1:4 DCM:hexanes to afford a further 0.71 g (9%) of the title compound. 1H NMR (300 MHz, CDCl3): δ 8.99 (s, 1H), 7.95 (d, J=8.4, 1H), 7.77 (d, J=8.4 Hz, 1H).

後処理

  1. additionwas added dropwise to the reaction mixture
  2. customthe internal temperature below 5° C
  3. stirringThe mixture was stirred for further 10 min
  4. stirringwas stirred vigorously for 10 min
  5. customThe solid formed
  6. extractionwas extracted with ethyl acetate (3×70 mL)
  7. washThe combined organic fractions were washed with water (100 mL)
  8. dry with materialdried over anhydrous sodium sulfate
  9. concentrationconcentrated
  10. customPurification of the residue by column chromatography (25% ethyl acetate:hexanes)

出典と根拠

ORDレコード
ord-c0b285f54991407c8be56ed931932c99
出典データセット
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08378104B2

反応ノート

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