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Cyclopropylamine → 5-bromo-N-cyclopropyl-2,3-dimethylbenzamide

HRID 337615
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HRID 337615 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH3:12])[C:5]([CH3:11])=[C:6]([CH:10]=1)[C:7]([OH:9])=O.CN(C(ON1N=NC2[CH:24]=[CH:25][CH:26]=[N:27]C1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C1(N)CC1.CCN(C(C)C)C(C)C>CN(C=O)C>[Br:1][C:2]1[CH:3]=[C:4]([CH3:12])[C:5]([CH3:11])=[C:6]([CH:10]=1)[C:7]([NH:27][CH:26]1[CH2:24][CH2:25]1)=[O:9]
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참가 물질

6

반응물 4

HCID 69828CyclopropylamineHCID 81531DiisopropylethylamineHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 668959895-Bromo-2,3-dimethylbenzoic acid

생성물 1

HCID 670621395-bromo-N-cyclopropyl-2,3-dimethylbenzamide

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매

실험 절차

To a stirred DMF (0.2 M) solution of 5-bromo-2,3-dimethylbenzoic acid (1 eq.) from the previous step was added HATU (1.3 eq.), cyclopropylamine (1.2 eq.) and Hunig's base (3 eq.). The resulting reaction mixture was stirred at RT for 18 h. The reaction was then quenched with saturated aqueous ammonium chloride and extracted with EtOAc. The combined organic extracts were washed further with water and brine, dried over Na2SO4, filtered and the filtrate concentrated in vacuo. Purification of the crude product thus obtained by way of flash chromatography (SiO2, 7:3 (v/v) Hex:EtOAc→EtOAc) afforded the title compound as a white solid.

후처리

  1. customThe resulting reaction mixture
  2. customThe reaction was then quenched with saturated aqueous ammonium chloride
  3. extractionextracted with EtOAc
  4. washThe combined organic extracts were washed further with water and brine
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationthe filtrate concentrated in vacuo
  8. customPurification of the crude product
  9. customthus obtained by way of flash chromatography (SiO2, 7:3 (v/v) Hex:EtOAc→EtOAc)

출처 및 근거

ORD 기록
ord-da10b6e5a0284a9a9d55f06727581f78
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08889714B2

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