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Dimethyl-1,3-thiazole-5-carboxylic acid → 2-[2-(3-Butyl-5-methyl-isoxazol-4-yl)-2-hydroxy-ethyl]-4-methyl-thiazole-5-carboxylic acid methyl ester

HRID 1923606
ノート
印刷プレビュー

反応式

HRID 1923606 の反応式
[CH3:1][C:2]1[S:3][C:4]([C:8]([OH:10])=[O:9])=[C:5]([CH3:7])[N:6]=1.[CH2:11]([Li])CCC.[CH2:16]([C:20]1[C:24]([CH:25]=[O:26])=[C:23]([CH3:27])[O:22][N:21]=1)[CH2:17][CH2:18][CH3:19]>C1COCC1.CCCCCC>[CH3:11][O:9][C:8]([C:4]1[S:3][C:2]([CH2:1][CH:25]([C:24]2[C:20]([CH2:16][CH2:17][CH2:18][CH3:19])=[N:21][O:22][C:23]=2[CH3:27])[OH:26])=[N:6][C:5]=1[CH3:7])=[O:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 736488Dimethyl-1,3-thiazole-5-carboxylic acidHCID 866443693-Butyl-5-methyl-isoxazole-4-carbaldehydeHCID 178418339Butyllithium

生成物 1

HCID 666436972-[2-(3-Butyl-5-methyl-isoxazol-4-yl)-2-hydroxy-ethyl]-4-methyl-thiazole-5-carboxylic acid methyl ester収率 79%

試薬・触媒・溶媒 2

HCID 8028Tetrahydrofuran溶媒2 回
HCID 8058Hexane溶媒

実験手順

To a stirred solution of 2,4-dimethyl-thiazole-5-carboxylic acid (7.52 g, 47.8 mmol) in THF (400 mL) at −78° C. and under argon was added n-butyllithium (59.8 mL of a 1.60M solution in hexane, 95.7 mmol) dropwise. After 1.5 h, a solution of 3-butyl-5-methyl-isoxazole-4-carbaldehyde (8.0 g, 47.8 mmol) in THF (200 mL) was added dropwise over 30 min. After 3 h the reaction mixture was quenched with HCl (1 N, 80 mL) and water (100 mL), warmed to room temperature, then the reaction mixture was adjusted to pH 6 with 10% aqueous citric acid. The reaction mixture was concentrated to remove most of the THF then was extracted with ethyl acetate. The combined extracts were dried, filtered and concentrated. The resultant oil was redissolved in methanol (400 mL) and ether (200 mL) then (trimethylsilyl)diazomethane (71.8 ml, of a 2M solution in ether, 144 mmol) was added dropwise. After 30 min, further (trimethylsilyl)diazomethane (71.8 mL of a 2M solution in ether, 144 mmol) was added. After 30 min, the reaction mixture was quenched with acetic acid then saturated aqueous sodium bicarbonate (200 mL) added. The mixture was filtered and the filtrates concentrated to ˜200 mL then extracted with in ethyl acetate. The combined organic extracts were dried, filtered and concentrated then purified by chromatography (silica, 10 to 40% ethyl acetate in heptane) to give the title compound (12.8 g, 79%) as a yellow solid. MS: m/e=321.2 [M+H—H2O]+.

後処理

  1. customAfter 3 h the reaction mixture was quenched with HCl (1 N, 80 mL) and water (100 mL)
  2. concentrationThe reaction mixture was concentrated
  3. customto remove most of the THF
  4. extractionthen was extracted with ethyl acetate
  5. customThe combined extracts were dried
  6. filtrationfiltered
  7. concentrationconcentrated
  8. dissolutionThe resultant oil was redissolved in methanol (400 mL)
  9. additionether (200 mL) then (trimethylsilyl)diazomethane (71.8 ml, of a 2M solution in ether, 144 mmol) was added dropwise
  10. waitAfter 30 min
  11. additionfurther (trimethylsilyl)diazomethane (71.8 mL of a 2M solution in ether, 144 mmol) was added
  12. waitAfter 30 min
  13. customthe reaction mixture was quenched with acetic acid
  14. additionsaturated aqueous sodium bicarbonate (200 mL) added
  15. filtrationThe mixture was filtered
  16. concentrationthe filtrates concentrated to ˜200 mL
  17. extractionthen extracted with in ethyl acetate
  18. customThe combined organic extracts were dried
  19. filtrationfiltered
  20. concentrationconcentrated
  21. customthen purified by chromatography (silica, 10 to 40% ethyl acetate in heptane)

出典と根拠

ORDレコード
ord-928451f5bf3c4de3976df4f2d9dee404
出典データセット
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08178522B2

反応ノート

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