Dimethyl Sulfoxide → 3-(2-Methyl-pyrimidin-5-yl)-5-oxo-pentanoic acid ethyl ester

HRID 1827681노트

반응식

HRID 1827681 반응식
C(Cl)(=O)C(Cl)=O.CS(C)=O.[CH2:11]([O:13][C:14](=[O:27])[CH2:15][CH:16]([C:20]1[CH:21]=[N:22][C:23]([CH3:26])=[N:24][CH:25]=1)[CH2:17][CH2:18][OH:19])[CH3:12].CCN(CC)CC>C(Cl)Cl>[CH2:11]([O:13][C:14](=[O:27])[CH2:15][CH:16]([C:20]1[CH:21]=[N:22][C:23]([CH3:26])=[N:24][CH:25]=1)[CH2:17][CH:18]=[O:19])[CH3:12]

참가 물질

6

반응물 4

HCID 679Dimethyl SulfoxideHCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 235812815-Hydroxy-3-(2-methyl-pyrimidin-5-yl)-pentanoic acid ethyl ester

생성물 1

HCID 235812803-(2-Methyl-pyrimidin-5-yl)-5-oxo-pentanoic acid ethyl ester

시약·촉매·용매 1

HCID 6344Dichloromethane용매3회

실험 절차

To a solution of oxalyl chloride (73 μL, 0.84 mmol) in CH2Cl2 at −78° C. was added DMSO (80 μL, 1.0 mmol) dropwise. After gas evolution ceased, 4-5 (100 mg, 0.42 mmol) in CH2Cl2 was added. After 30 minutes, the cooling bath was removed and NEt3 (290 μL, 2.1 mmol) was added. After 20 minutes, the reaction mixture was diluted with CH2Cl2 and washed sat. NaHCO3 and brine, dried (MgSO4), and concentrated to give 4-6 as a yellow oil.

후처리

  1. customthe cooling bath was removed
  2. waitAfter 20 minutes
  3. washwashed sat. NaHCO3 and brine
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-5d578c0639a048f299215ecf89fa54d3
출처 데이터셋
uspto-grants-2006_06
특허 번호
US07056909B2

반응 노트

불러오는 중…