Acetic Acid → Methyl 5-(2-(((4-bromo-3-fluorophenyl)amino)methyl)-5-fluorophenyl)picolinate

HRID 405169노트

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HRID 405169 반응식
[BH-](OC(C)=O)(OC(C)=O)OC(C)=O.[Na+].[F:15][C:16]1[CH:17]=[CH:18][C:19]([CH:32]=O)=[C:20]([C:22]2[CH:23]=[CH:24][C:25]([C:28]([O:30][CH3:31])=[O:29])=[N:26][CH:27]=2)[CH:21]=1.[Br:34][C:35]1[CH:41]=[CH:40][C:38]([NH2:39])=[CH:37][C:36]=1[F:42].CC(O)=O>CCOC(C)=O.ClCCCl>[Br:34][C:35]1[CH:41]=[CH:40][C:38]([NH:39][CH2:32][C:19]2[CH:18]=[CH:17][C:16]([F:15])=[CH:21][C:20]=2[C:22]2[CH:23]=[CH:24][C:25]([C:28]([O:30][CH3:31])=[O:29])=[N:26][CH:27]=2)=[CH:37][C:36]=1[F:42]

참가 물질

7

반응물 4

HCID 176Acetic AcidHCID 8218484-Bromo-3-fluoroanilineHCID 5049666Sodium triacetoxyborohydrideHCID 86674254HCID 86674254, 화합물

생성물 1

HCID 71060114Methyl 5-(2-(((4-bromo-3-fluorophenyl)amino)methyl)-5-fluorophenyl)picolinate

시약·촉매·용매 2

HCID 111,2-Dichloroethane용매HCID 8857Ethyl Acetate용매

실험 절차

Solid NaBH(OAc)3 (491 mg, 2.3 mmol) was added to a DCE solution (4 mL) of methyl 5-(5-fluoro-2-formylphenyl)picolinate (300 mg, 1.2 mmol), 4-bromo-3-fluoroaniline (242 mg, 1.3 mmol), and AcOH (0.27 mL, 4.6 mmol) and the resulting mixture was stirred at room temperature. After 16 h the resulting mixture diluted with EtOAc washed with water and brine, dried (Na2SO4), concentrated and purified via column chromatography to yield the title compound.

후처리

  1. washwashed with water and brine
  2. dry with materialdried (Na2SO4)
  3. concentrationconcentrated
  4. custompurified via column chromatography

출처 및 근거

ORD 기록
ord-8962f3de38a84cb48e0ff9f948ad15f3
출처 데이터셋
uspto-grants-2014_06
특허 번호
US08748624B2

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