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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
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HRID 1923542 반응식
[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]
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참가 물질

5

반응물 3

HCID 736488Dimethyl-1,3-thiazole-5-carboxylic acidHCID 2724682Lithium diisopropylamideHCID 66643618HCID 66643618, 화합물

생성물 1

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

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매3회

실험 절차

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]+.

후처리

  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)

출처 및 근거

ORD 기록
ord-fad7cd87b78c4bd0ac9d72cf5c5b1e70
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08178522B2

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