Dimethylformamide → 3-methoxy-2,2-dimethylpropionic acid 5-[[3-(2-acetoxyethoxy)-2-fluoro-5-methoxyphenyl]-(4-{amino[2-methylall yloxycarbonylimino]methyl}phenylamino)methyl]-2-pyrimidin-2-yl-2H-[1,2,4]triazol-3-yloxymethyl ester

HRID 2089639

反応式

HRID 2089639 の反応式
C(O)(=O)C.[C:5]([O:8][CH2:9][CH2:10][O:11][C:12]1[C:13]([F:53])=[C:14]([CH:20]([NH:43][C:44]2[CH:49]=[CH:48][C:47]([C:50](=[NH:52])[NH2:51])=[CH:46][CH:45]=2)[C:21]2[N:22]=[C:23]([O:32][CH2:33][O:34][C:35](=[O:42])[C:36]([CH3:41])([CH3:40])[CH2:37][O:38][CH3:39])[N:24]([C:26]3[N:31]=[CH:30][CH:29]=[CH:28][N:27]=3)[N:25]=2)[CH:15]=[C:16]([O:18][CH3:19])[CH:17]=1)(=[O:7])[CH3:6].C(N(CC)CC)C.[N+](C1C=CC([O:70][C:71](=O)[O:72][CH2:73][C:74]([CH3:76])=[CH2:75])=CC=1)([O-])=O.CN(C=O)C>O.C(OCC)(=O)C>[C:5]([O:8][CH2:9][CH2:10][O:11][C:12]1[C:13]([F:53])=[C:14]([CH:20]([NH:43][C:44]2[CH:49]=[CH:48][C:47]([C:50]([NH2:51])=[N:52][C:71]([O:72][CH2:73][C:74]([CH3:76])=[CH2:75])=[O:70])=[CH:46][CH:45]=2)[C:21]2[N:22]=[C:23]([O:32][CH2:33][O:34][C:35](=[O:42])[C:36]([CH3:41])([CH3:40])[CH2:37][O:38][CH3:39])[N:24]([C:26]3[N:31]=[CH:30][CH:29]=[CH:28][N:27]=3)[N:25]=2)[CH:15]=[C:16]([O:18][CH3:19])[CH:17]=1)(=[O:7])[CH3:6]

参加物

7

反応物 4

HCID 6228DimethylformamideHCID 8471TriethylamineHCID 67469869Carbonic acid 2-methylallyl ester 4-nitrophenyl esterHCID 674699453-methoxy-2,2-dimethylpropionic acid 5-[[3-(2-acetoxyethoxy)-2-fluoro-5-methoxyphenyl]-(4-carbamimidoylphen ylamino)methyl]-2-pyrimidin-2-yl-2H-[1,2,4]triazol-3-yloxymethyl ester acetate

生成物 1

HCID 682128653-methoxy-2,2-dimethylpropionic acid 5-[[3-(2-acetoxyethoxy)-2-fluoro-5-methoxyphenyl]-(4-{amino[2-methylall yloxycarbonylimino]methyl}phenylamino)methyl]-2-pyrimidin-2-yl-2H-[1,2,4]triazol-3-yloxymethyl ester収率 95.1%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 8857Ethyl Acetate溶媒

実験手順

A mixture of 3-methoxy-2,2-dimethylpropionic acid 5-[[3-(2-acetoxyethoxy)-2-fluoro-5-methoxyphenyl]-(4-carbamimidoylphen ylamino)methyl]-2-pyrimidin-2-yl-2H-[1,2,4]triazol-3-yloxymethyl ester acetate (13 mg), triethylamine (0.0074 mL), carbonic acid 2-methylallyl ester 4-nitrophenyl ester (5.6 mg), and DMF (2 mL) was stirred for 3 days at room temperature. The resulting mixture was poured into ethyl acetate (100 mL) and water (30 mL). After shaking the mixture, the organic layer was collected, sequentially washed twice with water (30 mL) and with saturated aqueous sodium chloride solution (30 mL), and dried over anhydrous magnesium sulfate. The resulting mixture was filtered, and the filtrate obtained was concentrated under reduced pressure. The residue obtained was purified by NAM silica gel column chromatography (mixed solvent of methanol-ethyl acetate) to obtain the captioned compound (13 mg).

後処理

  1. stirringAfter shaking the mixture
  2. customthe organic layer was collected
  3. washsequentially washed twice with water (30 mL) and with saturated aqueous sodium chloride solution (30 mL)
  4. dry with materialdried over anhydrous magnesium sulfate
  5. filtrationThe resulting mixture was filtered
  6. customthe filtrate obtained
  7. concentrationwas concentrated under reduced pressure
  8. customThe residue obtained
  9. customwas purified by NAM silica gel column chromatography (mixed solvent of methanol-ethyl acetate)

出典と根拠

ORDレコード
ord-6455d7621b8f4b77aa4eb43a07109cc6
出典データセット
uspto-grants-2013_05
特許番号
US08436009B2

関連ノート

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