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Phosphorus oxychloride → 5,7-Dichlorothieno[2,3-c]pyridine

HRID 389525
ノート
印刷プレビュー

反応式

HRID 389525 の反応式
[Cl:1][C:2]1[N+:3]([O-])=[CH:4][CH:5]=[C:6]2[CH:10]=[CH:9][S:8][C:7]=12.O=P(Cl)(Cl)[Cl:14]>>[Cl:14][C:4]1[CH:5]=[C:6]2[CH:10]=[CH:9][S:8][C:7]2=[C:2]([Cl:1])[N:3]=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

3

反応物 2

HCID 24813Phosphorus oxychlorideHCID 86662415Thieno[2,3-c]pyridine, 7-chloro-, 6-oxide

生成物 1

HCID 714642675,7-Dichlorothieno[2,3-c]pyridine収率 70%

反応条件

温度
115 °C

実験手順

A mixture of 7-chlorothieno[2,3-c]pyridine 6-oxide (2.58 g, 13.8 mmol) and POCl3 (20 mL) was stirred at 115° C. under N2 for 7 h. After that time, the excess POCl3 was removed in vacuo, and the residue was poured into ice/water (100 mL), basified by addition of 8 N NaOH followed by saturated NaHCO3, and extracted with DCM (3×50 mL). The combined extracts were washed with saturated NaHCO3 (50 mL), water (50 mL) and brine (50 mL), dried over MgSO4, and concentrated in vacuo. The residue was purified by ISCO chromatography (0 to 40% EtOAc:heptane) to afford 1.97 g (70%) of the title compound as a beige solid. 1H NMR (400 MHz, DMSO-d6): δ 7.82 (d, J=5.6 Hz, 1 H), 7.68 (s, 1 H), 7.37 (d, J=5.6 Hz, 1 H); MS (ESI): 203.94, 205.94 [M+H]+; HPLC tR=1.55 min (TOF: polar—3 min).

後処理

  1. customAfter that time, the excess POCl3 was removed in vacuo
  2. additionthe residue was poured into ice/water (100 mL)
  3. additionbasified by addition of 8 N NaOH
  4. extractionextracted with DCM (3×50 mL)
  5. washThe combined extracts were washed with saturated NaHCO3 (50 mL), water (50 mL) and brine (50 mL)
  6. dry with materialdried over MgSO4
  7. concentrationconcentrated in vacuo
  8. customThe residue was purified by ISCO chromatography (0 to 40% EtOAc:heptane)

出典と根拠

ORDレコード
ord-6ab90584bfaf45d7ba7cb8f375c0eef3
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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