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Triethylamine → HCID 54439733, 화합물

HRID 728107
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HRID 728107 반응식
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([CH:17]=[CH:18][C:19]=1[N+:20]([O-:22])=[O:21])[CH:12]=[CH:13][C:14]([OH:16])=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(O)(=O)C.[NH2:27][CH:28]([C:30]1[CH:35]=[C:34]([CH3:36])[CH:33]=[CH:32][N:31]=1)[CH3:29].C1(N=C=NC2CCCCC2)CCCCC1.C(N(CC)CC)C>CN(C)C=O>[CH3:36][C:34]1[CH:33]=[CH:32][N:31]=[C:30]([CH:28]([NH:27][C:14](=[O:16])[CH:13]=[CH:12][C:11]2[CH:17]=[CH:18][C:19]([N+:20]([O-:22])=[O:21])=[C:9]([O:8][CH2:1][C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)[CH:10]=2)[CH3:29])[CH:35]=1
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참가 물질

6

반응물 4

HCID 8471TriethylamineHCID 10868DicyclohexylcarbodiimideHCID 543326493-Benzyloxy-4-nitrocinnamic acidHCID 67835920HCID 67835920, 화합물

생성물 1

HCID 54439733HCID 54439733, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a mixture of 3-benzyloxy-4-nitrocinnamic acid (12.9 g) and 2-(1-aminoethyl)-4-methylpyridine acetate (8.5 g) in N,N-dimethylformamide (150 ml) were added 1-hydroxybenzotraizole (7 g), N,N'-dicyclohexylcarbodiimide (10.65 g) and triethylamine (4.36 g), which was stirred at ambient temperature for 24 hours. After filtration, the filtrate was evaporated under reduced pressure. The residue was suspended in ethyl acetate (100 ml), which was filtered, and evaporated. The residue was subjected to column chromatography on silica gel to give 4-methyl-2-[1-(3-benzyloxy-4-nitrocinnamoylamino)ethyl]pyridine.

후처리

  1. filtrationAfter filtration
  2. customthe filtrate was evaporated under reduced pressure
  3. filtrationwhich was filtered
  4. customevaporated

출처 및 근거

ORD 기록
ord-5ff464cb50224c158dfa6a6a5780e6bb
출처 데이터셋
uspto-grants-1991_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05047411

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