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Triethylamine → HCID 178501061, 화합물

HRID 1893350
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HRID 1893350 반응식
[C:1](=[N:4][OH:5])([NH2:3])[CH3:2].C(N(CC)CC)C.[CH3:13][O:14][C:15]([C@H:17]1[CH2:22][CH2:21][C@H:20]([C:23](Cl)=O)[CH2:19][CH2:18]1)=[O:16]>O1CCCC1>[CH3:13][O:14][C:15]([C@H:17]1[CH2:22][CH2:21][C@H:20]([C:23]2[O:5][N:4]=[C:1]([CH3:2])[N:3]=2)[CH2:19][CH2:18]1)=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 30926N-HydroxyacetamidineHCID 178501148HCID 178501148, 화합물

생성물 1

HCID 178501061HCID 178501061, 화합물수율 89.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of acetamide oxime (0.19 g, 2.6 mmol) and triethylamine (0.36 ml, 2.6 mmol) in tetrahydrofuran (24 ml) was added trans-4-chlorocarbonyl-cyclohexanecarboxylic acid methyl ester (0.50 g, 2.4 mmol) at 0-5° C. After completed addition the cooling bath was removed, and the mixture was stirred for 30 minutes. The precipitated ammonium salts were removed by filtration and washed with tetrahydrofuran. The filtrate was concentrated to dryness. The residue was redissolved in 1,4-dioxane (24 ml). The mixture was treated with a catalytic amount of toluene-4-sulfonic acid monohydrate and heated at reflux over night (16 h). The solvent was evaporated. Flash-chromatography with n-heptane/ethyl acetate as eluent gave the title compound (0.48 g, 88%) as light brown oil. MS m/e: 225 ([M+H]+)

후처리

  1. additionaddition the cooling bath
  2. customwas removed
  3. customThe precipitated ammonium salts were removed by filtration
  4. washwashed with tetrahydrofuran
  5. concentrationThe filtrate was concentrated to dryness
  6. dissolutionThe residue was redissolved in 1,4-dioxane (24 ml)
  7. additionThe mixture was treated with a catalytic amount of toluene-4-sulfonic acid monohydrate
  8. temperatureheated
  9. temperatureat reflux over night (16 h)
  10. customThe solvent was evaporated

출처 및 근거

ORD 기록
ord-bb06ca2c1c6f4535954c842b5d027f2e
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08513238B2

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