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Ethyl 2-((2-bromo-6-nitrophenyl)thio)acetate → 8-Bromo-2H-benzo[b][1,4]thiazin-3(4H)-one

HRID 2175301
ノート
印刷プレビュー

反応式

HRID 2175301 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([N+:8]([O-])=O)[C:3]=1[S:11][CH2:12][C:13]([O:15]CC)=O>C(O)(=O)C.[Fe]>[Br:1][C:2]1[C:3]2[S:11][CH2:12][C:13](=[O:15])[NH:8][C:4]=2[CH:5]=[CH:6][CH:7]=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

4

反応物 1

HCID 70981689Ethyl 2-((2-bromo-6-nitrophenyl)thio)acetate

生成物 1

HCID 717427308-Bromo-2H-benzo[b][1,4]thiazin-3(4H)-one収率 93.3%

試薬・触媒・溶媒 2

HCID 23925Iron触媒HCID 176Acetic Acid溶媒

反応条件

温度
90 °C

実験手順

A mixture of ethyl 2-((2-bromo-6-nitrophenyl)thio)acetate (3.64 g, 11.37 mmol) and iron (6.35 g, 114 mmol) in acetic acid (56.8 ml) was stirred at 90° C. for 1.5 h and at room temperature overnight. The mixture was filtered through CELITE®, washed with methanol, followed by hot CHCl3:MeOH:AcOH (1:1:1) till most of the compound came off the CELITE®. The filtrated was concentrated and re-dissolved in EtOAc. The organic solution was washed with water, dried over MgSO4, filtered, and concentrated to afford the title compound (2.59 g, 90% yield). LCMS, [M+H]+=246.0. 1H NMR (400 MHz, DMSO-d6) δ 7.27 (dd, J=8.0, 1.0 Hz, 1H), 7.10 (t, J=8.0 Hz, 1H), 6.97 (dd, J=8.0, 1.0 Hz, 1H), 3.53 (s, 2H).

後処理

  1. filtrationThe mixture was filtered through CELITE®
  2. washwashed with methanol
  3. concentrationThe filtrated was concentrated
  4. dissolutionre-dissolved in EtOAc
  5. washThe organic solution was washed with water
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-326c67f919464544921fbf441a200905
出典データセット
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09062028B2

反応ノート

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