Water → Methyl 2,6-dichloro-4-cyanonicotinate

HRID 711438

반응식

HRID 711438 반응식
[Cl:1][C:2]1[N:11]=[C:10]([Cl:12])[CH:9]=[C:8](I)[C:3]=1[C:4]([O:6][CH3:7])=[O:5].[C:14]([Zn]C#N)#[N:15].O.CCOC(C)=O>CN(C=O)C.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[Cl:1][C:2]1[N:11]=[C:10]([Cl:12])[CH:9]=[C:8]([C:14]#[N:15])[C:3]=1[C:4]([O:6][CH3:7])=[O:5]

참가 물질

7

반응물 4

HCID 962WaterHCID 8857Ethyl AcetateHCID 58317523Methyl 2,6-dichloro-4-iodonicotinateHCID 178514179HCID 178514179, 화합물

생성물 1

HCID 58317683Methyl 2,6-dichloro-4-cyanonicotinate수율 40.3%

시약·촉매·용매 2

HCID 178418397HCID 178418397, 화합물촉매HCID 6228Dimethylformamide용매

반응 조건

온도
100 °C

실험 절차

A mixture of tetrakis(triphenylphosphine)palladium (34.8 mg, 0.03 mmol), methyl 2,6-dichloro-4-iodonicotinate (100 mg, 0.301 mmol) and dicyanozinc (38.9 mg, 0.331 mmol) in DMF (2 mL) was stirred at 100° C. overnight under N2 atmosphere. To the resulting mixture were added H2O and EtOAc. The aqueous phase was extracted with EtOAc, and the combined organic layers were washed with H2O and brine, dried over MgSO4 and evaporated. The residue was purified by chromatography on SiO2 to give the title compound as a white solid (28 mg, 40%). 1H NMR (500 MHz, DMSO-d6) δ ppm 3.99 (s, 3H), 8.44 (s, 1H).

후처리

  1. extractionThe aqueous phase was extracted with EtOAc
  2. washthe combined organic layers were washed with H2O and brine
  3. dry with materialdried over MgSO4
  4. customevaporated
  5. customThe residue was purified by chromatography on SiO2

출처 및 근거

ORD 기록
ord-1754059833614813b7ab368dda19dd23
출처 데이터셋
uspto-grants-2015_11
특허 번호
US09181255B2

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