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Dimethylformamide → HCID 86761668, 화합물

HRID 1875254
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HRID 1875254 반응식
[Li]CCCC.[Cl:6][C:7]1[N:8]=[C:9]([S:21]([N:24]([CH3:26])[CH3:25])(=[O:23])=[O:22])[N:10]([CH2:13][O:14][CH2:15][CH2:16][Si:17]([CH3:20])([CH3:19])[CH3:18])[C:11]=1Cl.CN([CH:30]=[O:31])C>C1COCC1>[Cl:6][C:7]1[N:8]=[C:9]([S:21]([N:24]([CH3:26])[CH3:25])(=[O:23])=[O:22])[N:10]([CH2:13][O:14][CH2:15][CH2:16][Si:17]([CH3:20])([CH3:19])[CH3:18])[C:11]=1[CH:30]=[O:31]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 70937249HCID 70937249, 화합물HCID 178418339Butyllithium

생성물 1

HCID 86761668HCID 86761668, 화합물수율 49.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

nBuLi (0.21 ml of a 2.4M solution in hex, 0.51 mmol) was added dropwise to a −78° C. solution of 4,5-dichloro-N,N-dimethyl-1-({[2-(trimethylsilyl)ethyl]oxy}methyl)-1H-imidazole-2-sulfonamide (0.18 g, 0.47 mmol) in THF (3 ml). The reaction mixture was stirred for 30 mins and DMF (0.4 ml, 5.17 mmol) was added. After 10 mins, the cooling bath was removed and the reaction mixture was warmed to RT. Sat'd NaHCO3 was added and the solution was extracted with EtOAc. The organic layer was dried (Na2SO4), filtered, evaporated, and purified by silica gel chromatography (0-20% EtOAc/hexanes) to provide the title compound (0.085 g, 49%) as a clear oil. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 9.93 (s, 1H), 5.94 (s, 2H), 3.63-3.70 (m, 2H), 3.09 (s, 6H), 0.89-0.98 (m, 2H), −0.02 (s, 9H).

후처리

  1. waitAfter 10 mins
  2. customthe cooling bath was removed
  3. additionSat'd NaHCO3 was added
  4. extractionthe solution was extracted with EtOAc
  5. dry with materialThe organic layer was dried (Na2SO4)
  6. filtrationfiltered
  7. customevaporated
  8. custompurified by silica gel chromatography (0-20% EtOAc/hexanes)

출처 및 근거

ORD 기록
ord-f683d8c8fd754c399358ce418b7f756c
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08304419B2

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