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Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl ester → Benzyl 4-[3-acetyl-2-(4-fluorophenyl)imidazo[1,2-a]pyridin-7-yl]piperidine-1-carboxylate

HRID 1785398
ノート
印刷プレビュー

反応式

HRID 1785398 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:9]=[C:10]3[CH:15]=[C:14]([CH:16]4[CH2:21][CH2:20][N:19]([C:22]([O:24][CH2:25][C:26]5[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=5)=[O:23])[CH2:18][CH2:17]4)[CH:13]=[CH:12][N:11]3[CH:32]=2)=[CH:4][CH:3]=1.[CH3:33][C:34](OCC1C2C(=CC=CC=2)C(COC(C)=O)=C2C=1C=CC=C2)=[O:35]>S(=O)(=O)(O)O>[C:34]([C:32]1[N:11]2[CH:12]=[CH:13][C:14]([CH:16]3[CH2:21][CH2:20][N:19]([C:22]([O:24][CH2:25][C:26]4[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=4)=[O:23])[CH2:18][CH2:17]3)=[CH:15][C:10]2=[N:9][C:8]=1[C:5]1[CH:6]=[CH:7][C:2]([F:1])=[CH:3][CH:4]=1)(=[O:35])[CH3:33]
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 2

HCID 613145Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl esterHCID 58774430Benzyl 4-[2-(4-fluorophenyl)imidazo[1,2-a]pyridin-7-yl]piperidine-1-carboxylate

生成物 1

HCID 58774431Benzyl 4-[3-acetyl-2-(4-fluorophenyl)imidazo[1,2-a]pyridin-7-yl]piperidine-1-carboxylate

試薬・触媒・溶媒 1

HCID 1118Sulfuric Acid触媒

反応条件

温度
140 °C

実験手順

Imidazopyridine 34 (290 mg, 0.675 mmol) was dissolved in acetic (50 mL) in a 250 mL round bottom flask. Three drops of sulfuric acid were then added, and the reaction was heated to 140° C. for 24 hours. The reaction was then concentrated under reduced pressure, then diluted with both ethyl acetate and saturated sodium bicarbonate solution, and extracted repeatedly into ethyl acetate. Organic fractions were pooled, dried over sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was then dissolved in 5 mL methylene chloride, then loaded onto a 40 g Isco RediSep normal phase silica cartridge, and purified on an Isco OptiX10 CombiFlash instrument using a gradient that started at 100% heptane and ended at 100% ethyl acetate. Fractions containing desired product were pooled and concentrated under reduced pressure. Yield of 35: 180 mg (56%). 1H NMR (400 MHz, CDCl3) δ 1.67 (m, 2H), 1.92 (m, 2H), 2.17 (s, 3H), 2.81 (m, 1H), 2.93 (bs, 2H), 4.38 (bs, 2H), 5.16 (s, 2H), 6.48 (d, J=7.2 Hz, 1H), 6.96 (t, J=8.8 Hz, 2H), 7.24 (m, 5H), 7.57 (s, 1H), 7.76 (m, 2H), 7.86 (d, J=7.2 Hz, 1H). MS (ESI+) 472.2.

後処理

  1. concentrationThe reaction was then concentrated under reduced pressure
  2. additiondiluted with both ethyl acetate and saturated sodium bicarbonate solution
  3. extractionextracted repeatedly into ethyl acetate
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. dissolutionThe crude product was then dissolved in 5 mL methylene chloride
  8. custompurified on an Isco OptiX10 CombiFlash instrument
  9. additionFractions containing desired product
  10. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-d22e45b0d2c44cec96c70cd36581360c
出典データセット
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07504501B2

反応ノート

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