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Methanol → (S)-2-(5-Amino-1-oxoisoquinolin-2(1H)-yl)-3-hydroxypropanamide

HRID 1161209
ノート
印刷プレビュー

反応式

HRID 1161209 の反応式
[OH:1][CH2:2][C@H:3]([N:7]1[CH:16]=[CH:15][C:14]2[C:9](=[CH:10][CH:11]=[CH:12][C:13]=2[N+:17]([O-])=O)[C:8]1=[O:20])[C:4]([NH2:6])=[O:5].CO>[Pd]>[NH2:17][C:13]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:14]=1[CH:15]=[CH:16][N:7]([C@@H:3]([CH2:2][OH:1])[C:4]([NH2:6])=[O:5])[C:8]2=[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

4

反応物 2

HCID 887MethanolHCID 59515781(S)-3-Hydroxy-2-(5-nitro-1-oxoisoquinolin-2(1H)-yl)propanamide

生成物 1

HCID 59515818(S)-2-(5-Amino-1-oxoisoquinolin-2(1H)-yl)-3-hydroxypropanamide

試薬・触媒・溶媒 1

HCID 23938Palladium触媒

実験手順

A round bottom flask (250 mL) was charged with (S)-3-hydroxy-2-(5-nitro-1-oxoisoquinolin-2(1H)-yl)propanamide (0.2 g, 0.0007 mol) and methanol (20 mL, 0.5 mol) and palladium, 10% weight on charcoal (0.02 g, 0.0001 mol) was added and the flask was evacuated of air with the aid of vaccum and the reaction was stirred under an atmosphere of hydrogen (1 atm) with the aid of a balloon. The reaction was stirred for 45 minutes, in which time the reaction was complete. The reaction was filtered and the solvent removed under reduced pressure to yield the pure product as a light yellow solid. MS m/z=248.3 (M+H).

後処理

  1. additionwas added
  2. customthe flask was evacuated of air with the aid of vaccum
  3. stirringThe reaction was stirred for 45 minutes, in which time the reaction
  4. filtrationThe reaction was filtered
  5. customthe solvent removed under reduced pressure

出典と根拠

ORDレコード
ord-6d528be8c6e3451aaf539c3840ff55a5
出典データセット
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07816371B2

反応ノート

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