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Sodium Carbonate → 5-[(2H-[1,3]Dioxolo[4,5-g]isoquinolin-5-yl)amino]pentan-1-ol

HRID 1579984
ノート
印刷プレビュー

反応式

HRID 1579984 の反応式
Cl[C:2]1[C:11]2[C:6](=[CH:7][C:8]3[O:14][CH2:13][O:12][C:9]=3[CH:10]=2)[CH:5]=[CH:4][N:3]=1.[OH:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][NH2:21].C(=O)([O-])[O-].[Na+].[Na+]>CO>[OH:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][NH:21][C:2]1[C:11]2[C:6](=[CH:7][C:8]3[O:14][CH2:13][O:12][C:9]=3[CH:10]=2)[CH:5]=[CH:4][N:3]=1
参加物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 10340Sodium CarbonateHCID 756345-Aminopentan-1-olHCID 21192459HCID 21192459、化合物

生成物 1

HCID 215647615-[(2H-[1,3]Dioxolo[4,5-g]isoquinolin-5-yl)amino]pentan-1-ol

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A mixture of 1.8 g. of 1-chloro-6,7-methylenedioxyisoquinoline and 5 g. of 5-hydroxypentylamine is heated at 140°C. for 5.5 hours. The resulting material is dissolved in methanol, sodium carbonate added and the resulting mixture refluxed for 15 minutes. The resulting mixture is filtered and evaporated in vacuo to an oil which is dissolved in chloroform. The resulting solution is evaporated in vacuo and the residue purified by chromatography over silica gel. The resulting oily product is then crystallized from ethanol/ethyl acetate and recrystallized from ethyl acetate/methanol to obtain 1-(5-hydroxypentyl)amino-6,7-methylenedioxyisoquinoline, m.p. 132.5°-134°C.

後処理

  1. additionA mixture of 1.8 g
  2. temperaturethe resulting mixture refluxed for 15 minutes
  3. filtrationThe resulting mixture is filtered
  4. customevaporated in vacuo to an oil which
  5. dissolutionis dissolved in chloroform
  6. customThe resulting solution is evaporated in vacuo
  7. customthe residue purified by chromatography over silica gel
  8. customThe resulting oily product is then crystallized from ethanol/ethyl acetate
  9. customrecrystallized from ethyl acetate/methanol

出典と根拠

ORDレコード
ord-e4e8ef35787e4436bea47879c83bf3d8
出典データセット
uspto-grants-1976_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03932412

反応ノート

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