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Hydroxyamine hydrochloride → HCID 178471206、化合物

HRID 2383316
ノート
印刷プレビュー

反応式

HRID 2383316 の反応式
[C:1]([C:3]1[C:4]([CH3:28])=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]([CH2:13][CH2:14][CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])[N:8]([C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])[CH2:7][CH2:6]2)#[N:2].Cl.[NH2:30][OH:31].C(=O)(O)[O-].[Na+]>C(O)C>[CH2:19]([O:18][C:16](=[O:17])[CH2:15][CH2:14][CH2:13][CH:9]1[C:10]2[C:5](=[C:4]([CH3:28])[C:3]([C:1]([NH:30][OH:31])=[NH:2])=[CH:12][CH:11]=2)[CH2:6][CH2:7][N:8]1[C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])[CH3:20]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 443297Hydroxyamine hydrochloride4 回HCID 516892Sodium Bicarbonate4 回HCID 595910941,1-Dimethylethyl 6-cyano-1-[4-(ethyloxy)-4-oxobutyl]-5-methyl-3,4-dihydro-2(1H)-isoquinolinecarboxylate

生成物 1

HCID 178471206HCID 178471206、化合物収率 86.4%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
80 °C

実験手順

A mixture of 1,1-dimethylethyl 6-cyano-1-[4-(ethyloxy)-4-oxobutyl]-5-methyl-3,4-dihydro-2(1H)-isoquinolinecarboxylate (Preparation 26; 533 mg, 1.38 mmol), hydroxylamine hydrochloride (575 mg, 8.27 mmol) and sodium bicarbonate (695 mg, 8.27 mmol) in ethanol (15 ml) was stirred at 80° C. for 32 h. More hydroxylamine hydrochloride and sodium bicarbonate (3 equivalent of each) were added, and heating was continued at 80° C. overnight. More hydroxylamine hydrochloride and sodium bicarbonate (3 equivalent of each) were added, and heating was continued at 80° C. for 5.5 h. More hydroxylamine hydrochloride and sodium bicarbonate (3 equivalent of each) were added, and heating was continued at 80° C. overnight. The mixture was cooled to room temperature and the solid was filtered off and washed with ethanol. The filtrate and washings were combined, most of the solvent removed, and the residue dissolved in ethyl acetate. The solution was washed with brine, dried over MgSO4 and concentrated in vacuo to give the title compound (500 mg) as a pale yellow foam.

後処理

  1. temperatureheating
  2. waitwas continued at 80° C. overnight
  3. temperatureheating
  4. waitwas continued at 80° C. for 5.5 h
  5. temperatureheating
  6. waitwas continued at 80° C. overnight
  7. temperatureThe mixture was cooled to room temperature
  8. filtrationthe solid was filtered off
  9. washwashed with ethanol
  10. customremoved
  11. dissolutionthe residue dissolved in ethyl acetate
  12. washThe solution was washed with brine
  13. dry with materialdried over MgSO4
  14. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-f986d637a14f46a185fb6eafe5726ecc
出典データセット
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08263620B2

反応ノート

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