Sodium hydride → HCID 71270138、化合物

HRID 927079ノート

反応式

HRID 927079 の反応式
[H-].[Na+].[I-].[CH3:4][S+](C)(C)=O.[CH2:9]([O:16][C:17]1[N:18]=[N:19][C:20]([C:31]([C:33]2[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=2)=[CH2:32])=[CH:21][C:22]=1[O:23][CH2:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>CS(C)=O.O1CCCC1>[CH2:9]([O:16][C:17]1[N:18]=[N:19][C:20]([C:31]2([C:33]3[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=3)[CH2:4][CH2:32]2)=[CH:21][C:22]=1[O:23][CH2:24][C:25]1[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=1)[C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1

参加物

6

実験手順

To a suspension of sodium hydride (0.487 g, 12.17 mmol, 60% in mineral oil) in DMSO (33.8 ml) stirring under nitrogen was added trimethyl sulfoxonium iodide (2.68 g, 12.17 mmol) in 4 portions over 20 minutes. A solution of 3,4-bis(benzyloxy)-6-(1-phenylethenyl)pyridazine (Intermediate 25; 3.2 g, 8.11 mmol) in tetrahydrofuran (50.7 ml) was added via a dropping funnel over 90 minutes before the reaction was left to stir at room temperature for 18 hours. The resulting mixture was concentrated, poured into ice water and extracted with ethyl acetate (×3). The organics portion was dried (MgSO4), filtered and concentrated to give a brown oil. The crude oil was purified by silica chromatography (eluting with 0-50% ethyl acetate in petrol) to yield 3,4-bis(benzyloxy)-6-(1-phenylcyclopropyl)pyridazine as a yellow oil (yield=23%).

後処理

  1. waitwas left
  2. stirringto stir at room temperature for 18 hours
  3. concentrationThe resulting mixture was concentrated
  4. additionpoured into ice water
  5. extractionextracted with ethyl acetate (×3)
  6. dry with materialThe organics portion was dried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customto give a brown oil
  10. customThe crude oil was purified by silica chromatography (eluting with 0-50% ethyl acetate in petrol)

出典と根拠

ORDレコード
ord-7ba4e5423ab94d1f85fbed25495a5411
出典データセット
uspto-grants-2016_03
特許番号
US09290456B2

反応ノート

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