Water → (S)-4-(5,7-dibromo-2,3-dihydro-1H-indol-1-yl)-1-[1-(methoxymethyl)-3-methoxypropyl]-6-methyl-1H-1,2,3-triazolo[4,5-c]pyridine

HRID 1066751ノート

反応式

HRID 1066751 の反応式
Cl[C:2]1[C:7]2[N:8]=[N:9][N:10]([C@H:11]([CH2:16][O:17][CH3:18])[CH2:12][CH2:13][O:14][CH3:15])[C:6]=2[CH:5]=[C:4]([CH3:19])[N:3]=1.[Br:20][C:21]1[CH:22]=[C:23]2[C:27](=[C:28]([Br:30])[CH:29]=1)[NH:26][CH2:25][CH2:24]2.C[Si]([N-][Si](C)(C)C)(C)C.[Na+].O>C1COCC1>[Br:20][C:21]1[CH:22]=[C:23]2[C:27](=[C:28]([Br:30])[CH:29]=1)[N:26]([C:2]1[C:7]3[N:8]=[N:9][N:10]([C@H:11]([CH2:16][O:17][CH3:18])[CH2:12][CH2:13][O:14][CH3:15])[C:6]=3[CH:5]=[C:4]([CH3:19])[N:3]=1)[CH2:25][CH2:24]2

参加物

6

反応条件

温度
25 °C

実験手順

(S)-4-chloro-1-(1-methoxymethyl-3-methoxypropyl)-6-methyl-1H-1,2,3-triazolo[4,5-c]pyridine (0.72 g, 2.54 mmol) and 5,7-dibromoindoline (0.72 g, 2.60 mmol) were dissolved in anhydrous THF (6 mL) and cooled in an ice bath. To that a 1 M solution of NaHMDS in THF (3.0 mL, 3.0 mmol) was added and the reaction was stirred for 20 min, allowed to warm to 25° C. and stirred for 3 h. Then water (30 mL) was added and the mixture was extracted twice with EtOAc (80 and 40 mL). The combined organic extracts was washed with brine (30 mL) dried (MgSO4) and stripped in vacuo. The residue was chromatographed on silica gel using 40% EtOAc/hexanes as eluent to give the product (1.14 g, 85% yield).

後処理

  1. temperaturecooled in an ice bath
  2. stirringstirred for 3 h
  3. extractionthe mixture was extracted twice with EtOAc (80 and 40 mL)
  4. washThe combined organic extracts was washed with brine (30 mL)
  5. dry with materialdried (MgSO4)
  6. customThe residue was chromatographed on silica gel using 40% EtOAc/hexanes as eluent

出典と根拠

ORDレコード
ord-d07436b75e014f1da87edb4857051949
出典データセット
uspto-grants-2001_06
特許番号
US06245769B1

反応ノート

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