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

HRID 1923542
ノート
印刷プレビュー

反応式

HRID 1923542 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.[Li+].CC([N-]C(C)C)C.[CH2:19]([C:23]1[C:27]([CH2:28]Cl)=[C:26]([CH3:30])[O:25][N:24]=1)[CH2:20][CH2:21][CH3:22]>C1COCC1>[CH2:19]([C:23]1[C:27]([CH2:28][CH2:1][C:2]2[S:3][C:4]([C:8]([OH:10])=[O:9])=[C:5]([CH3:7])[N:6]=2)=[C:26]([CH3:30])[O:25][N:24]=1)[CH2:20][CH2:21][CH3:22]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 736488Dimethyl-1,3-thiazole-5-carboxylic acidHCID 2724682Lithium diisopropylamideHCID 66643618HCID 66643618、化合物

生成物 1

HCID 666436692-[2-(3-Butyl-5-methyl-isoxazol-4-yl)-ethyl]-4-methyl-thiazole-5-carboxylic acid収率 68.1%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒3 回

実験手順

To a stirred solution of 2,4-dimethyl-thiazole-5-carboxylic acid (157 mg, 1.0 mmol) in THF (3 mL) at −78° C. and under argon was added LDA (1.0 mL of a 2M solution in THF, 2.0 mmol) dropwise. After 1.5 h a solution of 3-butyl-4-chloromethyl-5-methyl-isoxazole (188 mg, 1.0 mmol) in THF (2 mL) was added dropwise. After 1 h the reaction mixture was quenched with HCl (1 N, 10 mL) then warmed to room temperature and extracted with ethyl acetate. The combined extracts were dried, filtered and concentrated. Purification by chromatography (silica, 0 to 10% methanol in dichloromethane) gave the title compound (210 mg, 68%) as an off white solid. MS: m/e=307.3 [M+H]+.

後処理

  1. customAfter 1 h the reaction mixture was quenched with HCl (1 N, 10 mL)
  2. extractionextracted with ethyl acetate
  3. customThe combined extracts were dried
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customPurification by chromatography (silica, 0 to 10% methanol in dichloromethane)

出典と根拠

ORDレコード
ord-fad7cd87b78c4bd0ac9d72cf5c5b1e70
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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