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Thiophene → Cyclohexanecarboxylic acid [2-(2-amino-5-benzoyl-benzylamino)-ethyl]-amide

HRID 2088772
ノート
印刷プレビュー

反応式

HRID 2088772 の反応式
[NH2:1][C:2]1[CH:9]=[CH:8][C:7]([C:10](=[O:17])[C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH:6][C:3]=1[CH:4]=O.[NH2:18][CH2:19][CH2:20][NH:21][C:22]([CH:24]1[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]1)=[O:23].S1C=CC=C1>CO.[Pd]>[NH2:1][C:2]1[CH:9]=[CH:8][C:7]([C:10](=[O:17])[C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH:6][C:3]=1[CH2:4][NH:18][CH2:19][CH2:20][NH:21][C:22]([CH:24]1[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]1)=[O:23]
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 8030ThiopheneHCID 13028009N-(2-aminoethyl)cyclohexanecarboxamideHCID 586251382-Amino-5-benzoylbenzaldehyde

生成物 1

HCID 58625175Cyclohexanecarboxylic acid [2-(2-amino-5-benzoyl-benzylamino)-ethyl]-amide

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol
溶媒

実験手順

A mixture of 2-amino-5-benzoylbenzaldehyde (0.007 mol) and cyclohexanecarboxylic acid (2-amino-ethyl)-amide (0.007 mol) in methanol was hydrogenated at 50° C. with 10% Pd/C (0.5 g) as a catalyst in the presence of thiophene solution (1 mL). After uptake of H2 gas (1 equiv.) the catalyst was filtered off and the solvent evaporated. The residue was purified by column chromatography over silica gel (Biotage column) (eluent:CH2Cl2:methanol gradient). The desired fractions were collected and the solvent evaporated to yield the title compound as a residue.

後処理

  1. filtrationAfter uptake of H2 gas (1 equiv.) the catalyst was filtered off
  2. customthe solvent evaporated
  3. customThe residue was purified by column chromatography over silica gel (Biotage column) (eluent:CH2Cl2:methanol gradient)
  4. customThe desired fractions were collected
  5. customthe solvent evaporated

出典と根拠

ORDレコード
ord-938dfaba28374d9d966eb3d6747ff952
出典データセット
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08436006B2

反応ノート

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