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Ethoxalyl chloride → Ethyl 3-(3,5-dibromo-4-hydroxyphenyl)-1,2,4-oxadiazole-5-carboxylate

HRID 222353
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HRID 222353 반응식
Cl[C:2](=[O:8])[C:3]([O:5][CH2:6][CH3:7])=[O:4].[Br:9][C:10]1[CH:11]=[C:12]([CH:17]=[C:18]([Br:21])[C:19]=1[OH:20])[C:13](=[N:15]O)[NH2:14]>N1C=CC=CC=1>[Br:9][C:10]1[CH:11]=[C:12]([C:13]2[N:15]=[C:2]([C:3]([O:5][CH2:6][CH3:7])=[O:4])[O:8][N:14]=2)[CH:17]=[C:18]([Br:21])[C:19]=1[OH:20]
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참가 물질

4

반응물 2

HCID 20884Ethoxalyl chlorideHCID 46396913,5-Dibromo-N',4-dihydroxybenzimidamide

생성물 1

HCID 136139598Ethyl 3-(3,5-dibromo-4-hydroxyphenyl)-1,2,4-oxadiazole-5-carboxylate수율 46%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

Ethyl 2-chloro-2-oxoacetate (12.3 g, 82 mmol) was added dropwise to a stirred solution of 3,5-dibromo-N′,4-dihydroxybenzimidamide (25.5 g, 82 mmol) in pyridine (120 mL) and the mixture was stirred at room temperature for 1 hour and then at 60° C. for 2 hours. The resulting suspension was poured onto water (1.5 L) and extracted with ethyl acetate (2×400 mL). The combined extracts were washed with saturated sodium chloride, dried (MgSO4) and evaporated in vacuo to give an oily solid that was purified by flash chromatography to give a colourless powder. Crystallisation from toluene (400 mL) gave the title compound (I 4.7 g, 46%) as colourless crystals. 1H NMR δ (ppm) (DMSO-d6): 1.14 (3H, t), 4.49 (2H, q), 8.14 (2H, s), 10.93 (1H, br s).

후처리

  1. waitat 60° C. for 2 hours
  2. additionThe resulting suspension was poured onto water (1.5 L)
  3. extractionextracted with ethyl acetate (2×400 mL)
  4. washThe combined extracts were washed with saturated sodium chloride
  5. dry with materialdried (MgSO4)
  6. customevaporated in vacuo
  7. customto give an oily solid
  8. customthat was purified by flash chromatography
  9. customto give a colourless powder
  10. customCrystallisation from toluene (400 mL)

출처 및 근거

ORD 기록
ord-9702d39f347646e5a11fe6a7aafb4c87
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08207205B2

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