Triethylamine → 2-(4-Morpholinylcarbonyl)-1,3-thiazol-5-amine

HRID 1070624

반응식

HRID 1070624 반응식
[N:1]1([C:7](=[O:12])[C:8]([S:10][CH3:11])=S)[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.S(=O)(=O)(O)O.[NH2:18][CH2:19]C#N.C([N:24](CC)CC)C>CO>[N:1]1([C:7]([C:8]2[S:10][C:11]([NH2:24])=[CH:19][N:18]=2)=[O:12])[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 196971Aminoacetonitrile sulfate (1:1)HCID 22397235Methyl 4-morpholinyl(oxo)ethanedithioate

생성물 1

HCID 223972262-(4-Morpholinylcarbonyl)-1,3-thiazol-5-amine수율 31%

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

To a stirring mixture of methyl 4-morpholinyl(oxo)ethanedithioate (Preparation 25, 500 mg) and aminoacetonitrile bisulfate (564 mg) in MeOH (10 mL) at 0° C. is added triethylamine in MeOH (5 mL). The mixture is stirred overnight and allowed to warm to ambient temperature. The solution is filtered, and solvent removed from the filtrate. The residue is washed with water (15 mL) and extracted with EtOAc (3×20 mL), dried over MgSO4, and the solvent removed. The residue is purified by SiO2 flash column chromatography (eluent 3/1 EtOAc/hexane) to afford 161 mg (31%) of the title compound as a light brown solid. Physical characteristics: 1H NMR (CDCl3) δ3.78, 4.35, 7.05; IR (diffuse reflectance) 3321, 3217, 2858, 1580, 1438, 1418, 1348, 1276, 1178, 1113, 1003, 834, 783, 731, 619 cm−1; MS (ESI+) m/z 214 (M+H)+. Anal. Found: C, 45.24; H, 5.33; N, 19.42.

후처리

  1. filtrationThe solution is filtered
  2. customsolvent removed from the filtrate
  3. washThe residue is washed with water (15 mL)
  4. extractionextracted with EtOAc (3×20 mL)
  5. dry with materialdried over MgSO4
  6. customthe solvent removed
  7. customThe residue is purified by SiO2 flash column chromatography (eluent 3/1 EtOAc/hexane)

출처 및 근거

ORD 기록
ord-8b5410d9198848f39eb671481d19ace6
출처 데이터셋
uspto-grants-2005_06
특허 번호
US06903097B2

연결된 노트

불러오는 중…