Ammonium Chloride → HCID 59639533, 화합물

HRID 2250043노트

반응식

HRID 2250043 반응식
C1[O:18][CH2:17][CH2:16]OCCOCCOCCOCCOC1.COC(CP(=O)(OCC(F)(F)F)OCC(F)(F)F)=O.C[Si]([N-][Si](C)(C)C)(C)C.[K+].[NH2:48][C:49]1[C:54]([CH:55]=O)=[C:53]([C:57]2[CH:62]=[CH:61][CH:60]=[CH:59][C:58]=2[F:63])[N:52]=[C:51]([S:64][CH3:65])[N:50]=1.[NH4+].[Cl-]>C1(C)C=CC=CC=1.C1COCC1.CCOCC>[F:63][C:58]1[CH:59]=[CH:60][CH:61]=[CH:62][C:57]=1[C:53]1[C:54]2[CH:55]=[CH:16][C:17](=[O:18])[NH:48][C:49]=2[N:50]=[C:51]([S:64][CH3:65])[N:52]=1

참가 물질

9

반응물 5

HCID 25517Ammonium ChlorideHCID 2855718-Crown-6HCID 184894Nsc 634137HCID 3251421Potassium bis(trimethylsilyl)amideHCID 9856557HCID 9856557, 화합물

생성물 1

HCID 59639533HCID 59639533, 화합물수율 108.8%

시약·촉매·용매 3

HCID 1140Toluene용매HCID 3283Diethyl Ether용매HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of 18-crown-6 (422 mg, 1.6 mmol, 5 eq) and bis(2,2,2-trifluoroethyl) (methoxycarbonylmethyl)phosphonate (81 uL, 0.38 mmol, 1.2 eq) in anhyd THF (20 mL) was cooled to −78°, potassium bis(trimethylsilyl)amide (0.96 mL, 0.48 mmol, 1.5 eq) as a 0.5 mol solution in toluene was added. This solution was stirred for additional 30 min at −78° and 4-amino-6-(2-fluoro-phenyl)-2-methylsulfanyl-pyrimidine-5-carbaldehyde (85 mg, 0.32 mmol) in dry THF (1 mL) was added dropwise. The reaction mixture was then stirred for 8 h at −78° and warmed to 23°, and stirred 16 h. Saturated aq NH4Cl (5 mL), followed by Et2O (20 mL), was added. The layers were separated. The organic layer was washed with satd aq NaCl, dried (MgSO4), filtered and solvent was evaporated. The yellow residue was purified by Flash chromatography to afford 100 mg (91% yield) of 4-(2-fluoro-phenyl)-2-methylsulfanyl-8H-pyrido[2,3-d]pyrimidin-7-one. 1H-NMR δ 2.62 (s, 3H), 6.55 (d, 1H, J=9.9 Hz), 7.26 (m, 3H), 7.52 (m, 2H), 8.99 (br s, 1H). LC MS (m/e)=288 (MH+). Rt=1.75 min.

후처리

  1. stirringThe reaction mixture was then stirred for 8 h at −78°
  2. temperaturewarmed to 23°
  3. stirringstirred 16 h
  4. additionwas added
  5. customThe layers were separated
  6. washThe organic layer was washed with satd aq NaCl
  7. dry with materialdried (MgSO4)
  8. filtrationfiltered
  9. customsolvent was evaporated
  10. customThe yellow residue was purified by Flash chromatography

출처 및 근거

ORD 기록
ord-0429db8371ac44ce9851929f00f3b97d
출처 데이터셋
uspto-grants-2008_01
특허 번호
US07314934B2

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