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

HRID 389525
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HRID 389525 반응식
[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
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참가 물질

3

반응물 2

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

생성물 1

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

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온도
115 °C

실험 절차

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).

후처리

  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)

출처 및 근거

ORD 기록
ord-6ab90584bfaf45d7ba7cb8f375c0eef3
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08378104B2

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