Methyl 5-(3-((tert-butoxycarbonyl)amino)prop-1-yn-1-yl)furan-2-carboxylate → 5-(3-Tert-butoxycarbonylaminopropyl)-furan-2-carboxylic acid methyl ester

HRID 2298228ノート

反応式

HRID 2298228 の反応式
[CH3:1][O:2][C:3]([C:5]1[O:6][C:7]([C:10]#[C:11][CH2:12][NH:13][C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])=[CH:8][CH:9]=1)=[O:4]>CO.[Pd]>[CH3:1][O:2][C:3]([C:5]1[O:6][C:7]([CH2:10][CH2:11][CH2:12][NH:13][C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])=[CH:8][CH:9]=1)=[O:4]

参加物

4

反応物 1

HCID 53793873Methyl 5-(3-((tert-butoxycarbonyl)amino)prop-1-yn-1-yl)furan-2-carboxylate

生成物 1

HCID 536486615-(3-Tert-butoxycarbonylaminopropyl)-furan-2-carboxylic acid methyl ester収率 24.6%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

To a solution of 5-(3-tert-butoxycarbonylamino-prop-1-ynyl)-furan-2-carboxylic Acid methyl ester (1.69 g) in MeOH (50 mL) was added 10% palladium on carbon (850 mg) and the mixture was hydrogenated on a Parr shaker at 50 psi for 18 h. The catalyst was removed via filtration through Celite and the volatiles were concentrated in vacuo. Flash chromatography (hexanes:EtOAc 4:1) provided 5-(3-tert-butoxycarbonylaminopropyl)-furan-2-carboxylic Acid methyl ester (422 mg, MS 284 M+) followed by 5-(3-tert-butoxycarbonylamino-propyl)-tetrahydrofuran-2-carboxylic Acid methyl ester (903 mg).

後処理

  1. customThe catalyst was removed via filtration through Celite
  2. concentrationthe volatiles were concentrated in vacuo

出典と根拠

ORDレコード
ord-6cfff630f65c4f74837b057a3ccdd9d9
出典データセット
uspto-grants-2002_12
特許番号
US06492412B2

反応ノート

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