Methanol → 2-Chloro-4-iodo-6-methoxy-5-(methoxymethyl)pyridine

HRID 6224

反応式

HRID 6224 の反応式
[Cl:1][C:2]1[N:7]=[C:6]([O:8][CH3:9])[C:5]([CH:10]=[O:11])=[C:4]([I:12])[CH:3]=1.[CH2:13]([SiH](CC)CC)C.CO.FC(F)(F)C(O)=O.C([O-])(O)=O.[Na+]>CCOCC>[Cl:1][C:2]1[CH:3]=[C:4]([I:12])[C:5]([CH2:10][O:11][CH3:13])=[C:6]([O:8][CH3:9])[N:7]=1

参加物

7

反応条件

温度
25 °C

実験手順

To a mixture of 6-chloro-4-iodo-2-methoxy-3-pyridinecarboxaldehyde (1.07 g, 3.60 mmol), triethylsilane (0.86 mL, 5.40 mmol) and methanol (0.43 mL, 10.6 mmol) at 0° C. was added trifluoroacetic acid (2.2 mL, 28.6 mmol), and the resulting solution was stirred at 25° C. for 14 h. After dilution with ether (30 mL), saturated NaHCO3 was added until the aqueous phase was rendered basic. The aqueous layer was extracted with ether (10 mL), and the combined ether layers were washed with water (10 mL) and brine (10 mL), and dried (Na2SO4) Concentration gave the crude product which was purified by radial PLC (silica gel, 5% ethyl acetate/hexanes) to afford 2-chloro-4-iodo-6-methoxy-5-(methoxymethyl)pyridine as a white solid (1.05 g, 93%): mp 69°-72° C. Recrystallization from hexanes provided an analytical sample: mp 74°-75° C. 1H NMR (300 MHz, CDCl3)δ7.40 (S, lH), 4.53 (s, 2H), 3.96 (s, 3H), 3.42 (s, 3H); IR (nujol) 1550, 1300, 1115, 1090, 1020, 940, 905, 830, 720 cm-1.

後処理

  1. extractionThe aqueous layer was extracted with ether (10 mL)
  2. washthe combined ether layers were washed with water (10 mL) and brine (10 mL)
  3. customdried
  4. concentration(Na2SO4) Concentration
  5. customgave the crude product which
  6. customwas purified by radial PLC (silica gel, 5% ethyl acetate/hexanes)

出典と根拠

ORDレコード
ord-36aa6e8ebe7944bf8139e096653ebd8c
出典データセット
uspto-grants-1993_09
特許番号
US05247089

関連ノート

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