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Ammonium Chloride → HCID 117987829, 화합물

HRID 2206063
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HRID 2206063 반응식
CCN(C(C)C)C(C)C.CCCCCC.C([Li])CCC.[Br:21][C:22]1[CH:23]=[C:24]([F:30])[C:25]([O:28][CH3:29])=[N:26][CH:27]=1.[CH:31]1([CH:36]=[O:37])[CH2:35][CH2:34][CH2:33][CH2:32]1.[Cl-].[NH4+]>C1COCC1>[Br:21][C:22]1[C:23]([CH:36]([CH:31]2[CH2:35][CH2:34][CH2:33][CH2:32]2)[OH:37])=[C:24]([F:30])[C:25]([O:28][CH3:29])=[N:26][CH:27]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 25517Ammonium ChlorideHCID 70106CyclopentanecarbaldehydeHCID 81531DiisopropylethylamineHCID 148370115-Bromo-3-fluoro-2-methoxypyridineHCID 178418244HCID 178418244, 화합물

생성물 1

HCID 117987829HCID 117987829, 화합물수율 29.1%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

반응 조건

온도
-78 °C

실험 절차

To a solution of DIEA (0.827 mL) in THF (90 mL) was added 1.6 M n-butyllithium hexane solution (3.64 mL) at −78° C., and the mixture was stirred under argon atmosphere at −78° C. for 30 min. To the reaction mixture was added a solution of 5-bromo-3-fluoro-2-methoxypyridine (1.00 g) in THF (30 mL) at −78° C., and the mixture was stirred under argon atmosphere at −78° C. for 1 hr. To the reaction mixture was added cyclopentanecarbaldehyde (0.572 g) at −78° C., and the mixture was stirred under argon atmosphere at −78° C. for 1 hr. To the reaction mixture was added saturated aqueous ammonium chloride solution at −78° C., and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (430 mg).

후처리

  1. stirringthe mixture was stirred under argon atmosphere at −78° C. for 1 hr
  2. stirringthe mixture was stirred under argon atmosphere at −78° C. for 1 hr
  3. extractionthe mixture was extracted with ethyl acetate
  4. washThe organic layer was washed with saturated brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by silica gel column chromatography (ethyl acetate/hexane)

출처 및 근거

ORD 기록
ord-ec32e8677ef1416bb497deb3cd0f61a1
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09371320B2

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