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Trimethyl orthoformate → 7-Methoxycarbonylmethyl-2-(4-(4-phenylbenzoylamino)butyl)-1,2,3,4-tetrahydroisoquinoline

HRID 1003711
ノート
印刷プレビュー

反応式

HRID 1003711 の反応式
O.O.O.[N+]([O-])([O-])=O.[Tl+3].[N+]([O-])([O-])=O.[N+]([O-])([O-])=O.[CH:17]([O:22][CH3:23])([O:20]C)OC.Cl.[C:25]([C:28]1[CH:37]=[C:36]2[C:31]([CH2:32][CH2:33][N:34]([CH2:38][CH2:39][CH2:40][CH2:41][NH:42][C:43](=[O:56])[C:44]3[CH:49]=[CH:48][C:47]([C:50]4[CH:55]=[CH:54][CH:53]=[CH:52][CH:51]=4)=[CH:46][CH:45]=3)[CH2:35]2)=[CH:30][CH:29]=1)(=O)C>CO.ClCCl>[CH3:23][O:22][C:17]([CH2:25][C:28]1[CH:37]=[C:36]2[C:31]([CH2:32][CH2:33][N:34]([CH2:38][CH2:39][CH2:40][CH2:41][NH:42][C:43](=[O:56])[C:44]3[CH:45]=[CH:46][C:47]([C:50]4[CH:51]=[CH:52][CH:53]=[CH:54][CH:55]=4)=[CH:48][CH:49]=3)[CH2:35]2)=[CH:30][CH:29]=1)=[O:20]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 9005Trimethyl orthoformateHCID 11270721Nitric acid,thallium(3+) salt, trihydrate (9CI)HCID 1317217547-Acetyl-2-(4-(4-phenylbenzoylamino)butyl)-1,2,3,4-tetrahydroisoquinoline, hydrochloride

生成物 1

HCID 187970057-Methoxycarbonylmethyl-2-(4-(4-phenylbenzoylamino)butyl)-1,2,3,4-tetrahydroisoquinoline収率 30%

試薬・触媒・溶媒 2

HCID 887
Methanol
溶媒
HCID 6344Dichloromethane溶媒

実験手順

A mixture of thallium (III) nitrate trihydrate (0.73 g, 1.6 mmol), K10 clay (1.65 g) and trimethyl orthoformate (1.8 ml, 1.6 mmol) in methanol (3 ml) was stirred at room temperature for 15 min. The solvent was evaporated in vacuo and dichloromethane (5 ml) was added to the residue. To this mixture was added a solution of 7-acetyl-2-(4-(4-phenylbenzoylamino)butyl)-1,2,3,4-tetrahydroisoquinoline, hydrochloride (0.50 g, 1.1 mmol) in dichloromethane (15 ml) and the reaction mixture was stirred for 4 h. The suspended solid was removed by filtration and the filtrate was washed with saturated aqueous potassium carbonate (2×30 ml), then brine (30 ml). Drying (Na2SO4) and evaporation in vacuo afforded a yellow gum which was chromatographed on silica using 20-100% ethyl acetate--pentane gradient elution to afford the title compound as an off-white solid (0.15 g, 30%).

後処理

  1. customThe solvent was evaporated in vacuo and dichloromethane (5 ml)
  2. additionwas added to the residue
  3. customThe suspended solid was removed by filtration
  4. washthe filtrate was washed with saturated aqueous potassium carbonate (2×30 ml)
  5. customDrying
  6. custom(Na2SO4) and evaporation in vacuo
  7. customafforded a yellow gum which
  8. customwas chromatographed on silica using 20-100% ethyl acetate
  9. washpentane gradient elution

出典と根拠

ORDレコード
ord-541ee847a9484995948dd89a307411f6
出典データセット
uspto-grants-2000_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06046210

反応ノート

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