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3-(N-benzyloxycarbonylpyrrolidin-2-ylmethyl)-1H-indole → Ammonium Hydroxide

HRID 843974
ノート
印刷プレビュー

反応式

HRID 843974 の反応式
C([O:8]C([N:11]1[CH2:15][CH2:14][CH2:13][CH:12]1[CH2:16][C:17]1[C:25]2[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=2)[NH:19][CH:18]=1)=O)C1C=CC=CC=1>[Pd].C(O)C>[OH-:8].[NH4+:11].[NH:11]1[CH2:15][CH2:14][CH2:13][CH:12]1[CH2:16][C:17]1[C:25]2[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=2)[NH:19][CH:18]=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 1

HCID 120500533-(N-benzyloxycarbonylpyrrolidin-2-ylmethyl)-1H-indole

生成物 2

HCID 14923Ammonium HydroxideHCID 185089963-(pyrrolidin-2-ylmethyl)-1H-indole

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

実験手順

A mixture of the 3-(N-benzyloxycarbonylpyrrolidin-2-ylmethyl)-1H-indole (2.00 mmol) and 10% palladium on carbon (0.20 g) in absolute ethanol (15 mL) is shaken under a hydrogen atmosphere (3 atm) for 4 to 24 hours, depending on substrate. The resulting reaction mixture is filtered through diatomaceous earth, and the filtrate is evaporated under reduced pressure. The residue is column chromatographed using silica gel (approximately 50 g) and elution with a solution of methylene chloride:methanol:ammonium hydroxide [8:2:0.2] or other appropriate solvent system to afford the corresponding 3-(pyrrolidin-2-ylmethyl)-1H-indole.

後処理

  1. customThe resulting reaction mixture
  2. filtrationis filtered through diatomaceous earth
  3. customthe filtrate is evaporated under reduced pressure
  4. customchromatographed
  5. washsilica gel (approximately 50 g) and elution with a solution of methylene chloride

出典と根拠

ORDレコード
ord-4941373eaacc463fb1e7d3a5c159d82d
出典データセット
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06380233B1

反応ノート

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