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Diisopropylethylamine → 4-amino-N-(2,2-dimethyl-3-pyrrolidin-1-yl-propyl)-3-methoxy-benzamide

HRID 2234473
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HRID 2234473 반응식
[NH2:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=O)=[CH:4][C:3]=1[O:11][CH3:12].[CH3:13][C:14]([CH3:23])([CH2:17][N:18]1[CH2:22][CH2:21][CH2:20][CH2:19]1)[CH2:15][NH2:16].CCN(C(C)C)C(C)C.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F>CN(C=O)C>[NH2:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([NH:16][CH2:15][C:14]([CH3:23])([CH3:13])[CH2:17][N:18]2[CH2:22][CH2:21][CH2:20][CH2:19]2)=[O:8])=[CH:4][C:3]=1[O:11][CH3:12]
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참가 물질

6

반응물 4

HCID 81531DiisopropylethylamineHCID 2880572486-69-3HCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 45088486beta,beta-Dimethyl-1-pyrrolidinepropanamine

생성물 1

HCID 686858814-amino-N-(2,2-dimethyl-3-pyrrolidin-1-yl-propyl)-3-methoxy-benzamide

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A mixture of the 4-amino-3-methoxy-benzoic acid (Aldrich; 2 g, 12 mmol) and 2,2-dimethyl-3-pyrrolidin-1-yl-propan-1-amine (WO 2004033419; 2.1 g, 13.2 mmol) were dissolved in DMF (50 mL), and to the solution was added DIPEA (3.1 g, 4.2 mL). The reaction was cooled with an ice-bath, and to it was added, portionwise, HATU (5.02 g, 13.2 mmol). The reaction mixture was stirred at ambient temperature for 18 hours. The solvent was evaporated, and the residue was partitioned between Ethyl Acetate (100 mL), and saturated aqueous sodium carbonate solution (3×40 mL), washed with brine (3×40 mL), dried over anhydrous Magnesium sulphate, filtered, and the solvent evaporated. The residue was purified by chromatography on a silica column pre-conditioned with Ethyl acetate and eluted with 10% MeOH-DCM+1% NH3. Those fractions containing the desired product were combined and the solvent was evaporated to yield the title compound as a pale brown gum, which crystallised on standing. (500 mgs; 14%).

후처리

  1. temperatureThe reaction was cooled with an ice-bath
  2. additionto it was added
  3. customThe solvent was evaporated
  4. customthe residue was partitioned between Ethyl Acetate (100 mL), and saturated aqueous sodium carbonate solution (3×40 mL)
  5. washwashed with brine (3×40 mL)
  6. dry with materialdried over anhydrous Magnesium sulphate
  7. filtrationfiltered
  8. customthe solvent evaporated
  9. customThe residue was purified by chromatography on a silica column pre-conditioned with Ethyl acetate
  10. washeluted with 10% MeOH-DCM+1% NH3
  11. additionThose fractions containing the desired product
  12. customthe solvent was evaporated

출처 및 근거

ORD 기록
ord-84021aabb5324d7592f34bf22b9f6cfa
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07709471B2

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