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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Triethylene Glycol → 26-Aminocholesterol

HRID 327775
ノート
印刷プレビュー

反応式

HRID 327775 の反応式
O=[C:2]1[CH2:37][C@@H:36]2[C@:23]([CH3:40])([CH2:24][CH2:25][C@H:26]3[C@H:35]2[CH2:34][CH:33]=[C:32]2[C@:27]3([CH3:39])[CH2:28][CH2:29][C@H:30]([OH:38])[CH2:31]2)[C@H:3]1[C@H:4]([CH3:22])[CH2:5][CH2:6][CH2:7][C@@H:8]([CH3:21])[CH2:9][N:10]1C(=O)C2=CC=CC=C2C1=O.O.NN.[OH-].[K+].C(O)COCCOCCO>O>[NH2:10][CH2:9][C@@H:8]([CH2:7][CH2:6][CH2:5][C@H:4]([C@@H:3]1[C@:23]2([CH3:40])[C@H:36]([C@H:35]3[C@H:26]([CH2:25][CH2:24]2)[C@:27]2([CH3:39])[C:32]([CH2:31][C@H:30]([CH2:29][CH2:28]2)[OH:38])=[CH:33][CH2:34]3)[CH2:37][CH2:2]1)[CH3:22])[CH3:21]
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

6

反応物 4

HCID 8172Triethylene GlycolHCID 14797Potassium HydroxideHCID 24654Hydrazine hydrate (1:1)HCID 9832896(25R)-16-oxo-26-phthalimidocholesterol

生成物 1

HCID 12633026-Aminocholesterol収率 66%

試薬・触媒・溶媒 1

HCID 962
Water
溶媒

反応条件

温度
150 °C

実験手順

A mixture of (25R)-16-oxo-26-phthalimidocholesterol (5) (0.70 g, 1.32 mmoles), hydrazine monohydrate (5 ml, 102.8 mmoles), potassium hydroxide (2.85 g, 50.8 mmoles) and triethylene glycol (20 ml) was heated to 150° C. for 30 minutes, then heated to 200° C. over 2 hours during which time water vapor distilled out of the mixture. The reaction mixture was maintained at this temperature for about 16 hours, under nitrogen, until the reaction was complete as determined by thin layer chromatography. Thereafter, the reaction mixture was cooled, poured into water, and extracted with chloroform. The extract was washed with water, dried over sodium sulfate, and evaporated under reduced pressure. Chromatography of the residue on silica gel eluted with CHCl3 gave 0.34 g (66%) of (25R)-26-aminocholesterol. The product was recrystallized from methylene chloride-ether and was found to have a melting point of 150°-152° C.

後処理

  1. distillationvapor distilled out of the mixture
  2. temperatureThe reaction mixture was maintained at this temperature for about 16 hours, under nitrogen, until the reaction
  3. temperatureThereafter, the reaction mixture was cooled
  4. additionpoured into water
  5. extractionextracted with chloroform
  6. washThe extract was washed with water
  7. dry with materialdried over sodium sulfate
  8. customevaporated under reduced pressure
  9. washChromatography of the residue on silica gel eluted with CHCl3

出典と根拠

ORDレコード
ord-41677efc9a4f47708f28cc5fd24acaa9
出典データセット
uspto-grants-1993_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05274088

反応ノート

読み込み中…

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