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Diisopropylethylamine → (RS) ethyl 3-{5-[2-(3-acetoxy-4-nitrophenyl)-acetylamino]-pyridin-2-yl}-butanoate

HRID 49723
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HRID 49723 반응식
F[P-](F)(F)(F)(F)F.N1(OC(N(C)C)=[N+](C)C)C2N=CC=CC=2N=N1.[NH2:25][C:26]1[CH:27]=[CH:28][C:29]([CH:32]([CH3:39])[CH2:33][C:34]([O:36][CH2:37][CH3:38])=[O:35])=[N:30][CH:31]=1.C(N(C(C)C)CC)(C)C.[C:49]([O:52][C:53]1[CH:54]=[C:55]([CH2:62][C:63](O)=[O:64])[CH:56]=[CH:57][C:58]=1[N+:59]([O-:61])=[O:60])(=[O:51])[CH3:50]>CN(C)C=O>[C:49]([O:52][C:53]1[CH:54]=[C:55]([CH2:62][C:63]([NH:25][C:26]2[CH:27]=[CH:28][C:29]([CH:32]([CH3:39])[CH2:33][C:34]([O:36][CH2:37][CH3:38])=[O:35])=[N:30][CH:31]=2)=[O:64])[CH:56]=[CH:57][C:58]=1[N+:59]([O-:61])=[O:60])(=[O:51])[CH3:50]
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참가 물질

6

반응물 4

HCID 81531DiisopropylethylamineHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 17946639(3-Acetoxy-4-nitro-phenyl)acetic acidHCID 17946645ethyl (3RS)-3-(5-aminopyrid-2-yl)butyrate

생성물 1

HCID 17946656(RS) ethyl 3-{5-[2-(3-acetoxy-4-nitrophenyl)-acetylamino]-pyridin-2-yl}-butanoate

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

반응 조건

온도
30 °C

실험 절차

A solution of O-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (10.95 g) in dry dimethylformamide (20 mL) was added to a solution of (RS) ethyl 3-(5-aminopyrid-2-yl)butanoate (3.0 g, Reference Example 5), diisopropylethylamine (10 mL) and (3-acetoxy-4-nitro-phenyl)acetic acid (6.89 g, Reference Example 17) in dimethylformamide (90 mL) under a nitrogen atmosphere. After stirring at 30° C. for 24 hours the reaction mixture was evaporated and the residue was partitioned between ethyl acetate and 5% aqueous sodium bicarbonate. The organic phase was washed with water, then with brine, then dried over magnesium sulphate, then treated with decolourising charcoal followed by filtration and evaporation of the filtrate to give the title compound as a dark oil.

후처리

  1. customwas evaporated
  2. customthe residue was partitioned between ethyl acetate and 5% aqueous sodium bicarbonate
  3. washThe organic phase was washed with water
  4. dry with materialwith brine, then dried over magnesium sulphate
  5. additiontreated with decolourising charcoal
  6. filtrationfollowed by filtration and evaporation of the filtrate

출처 및 근거

ORD 기록
ord-9ba64a1116f449bb9ec1ca7dc4da51be
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06706738B2

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