Triethylamine → HCID 89579974, 화합물

HRID 928608노트

반응식

HRID 928608 반응식
[NH:1]1[CH2:6][CH2:5][CH:4]([CH2:7][OH:8])[CH2:3][CH2:2]1.Cl[C:10]1[C:11]2[C:20]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)=[CH:19][S:18][C:12]=2[N:13]=[C:14]([CH2:16][Cl:17])[N:15]=1.C(N(CC)CC)C>C(O)C>[Cl:17][CH2:16][C:14]1[N:15]=[C:10]([N:1]2[CH2:6][CH2:5][CH:4]([CH2:7][OH:8])[CH2:3][CH2:2]2)[C:11]2[C:20]([C:21]3[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=3)=[CH:19][S:18][C:12]=2[N:13]=1

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 4207714-PiperidinemethanolHCID 23726818HCID 23726818, 화합물

생성물 1

HCID 89579974HCID 89579974, 화합물수율 95.8%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

4-Piperidinemethanol (0.85 g) was added to a suspension of 4-chloro-2-(chloromethyl)-5-phenyl-thieno[2,3-d]pyrimidine (1.45 g) in ethanol (70 mL). Triethylamine (1.4 mL) was added and the mixture was stirred at room temperature for 24 hr. The solvent was evaporated and the residue was dissolved in water (100 mL) and ethyl acetate (100 mL). The layers were separated and the aqueous was extracted with ethyl acetate (2×100 mL). The combined organic layers were washed with brine (1×100 mL), dried (sodium sulfate), filtered and evaporated to give an off-white foam (1.76 g). This was purified by silica chromatography (50 g cartridge; eluent petroleum ether 40-60/ethyl acetate 0 to 50%; collection by UV trigger). Fractions corresponding to the main peak were combined and evaporated to give the target compound as a white foam (1.10 g). m/z [M+H]+373.9/375.9. Retention time 4.67 min (LCMS method+ve 6 min).

후처리

  1. customThe solvent was evaporated
  2. dissolutionthe residue was dissolved in water (100 mL)
  3. customThe layers were separated
  4. extractionthe aqueous was extracted with ethyl acetate (2×100 mL)
  5. washThe combined organic layers were washed with brine (1×100 mL)
  6. dry with materialdried (sodium sulfate)
  7. filtrationfiltered
  8. customevaporated

출처 및 근거

ORD 기록
ord-b03b6fbd4bfa42a4b744312720d82546
출처 데이터셋
uspto-grants-2016_03
특허 번호
US09290511B2

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