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Hydrochloric Acid → Hexanamide, 3-amino-N-cyclopropyl-2-hydroxy-, hydrochloride (1:1), (2S,3S)-

HRID 1173762
ノート
印刷プレビュー

反応式

HRID 1173762 の反応式
[CH:1]1([NH:4][C:5]([CH:7]2[O:11]C(C)=[N:9][CH:8]2[CH2:13][CH2:14][CH3:15])=[O:6])[CH2:3][CH2:2]1.[ClH:16]>CO>[ClH:16].[CH:1]1([NH:4][C:5](=[O:6])[C@@H:7]([OH:11])[C@@H:8]([NH2:9])[CH2:13][CH2:14][CH3:15])[CH2:3][CH2:2]1
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 313Hydrochloric AcidHCID 68745903HCID 68745903、化合物

生成物 1

HCID 25067786Hexanamide, 3-amino-N-cyclopropyl-2-hydroxy-, hydrochloride (1:1), (2S,3S)-収率 28%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

N-Cyclopropyl-2-methyl-4-propyl-4,5-dihydro-1,3-oxazole-5-carboxamide (0.10 g, 0.5 mmol), methanol (4 ml) and concentrated hydrochloric acid (0.5 ml, 5.5 mmol) were mixed, and the mixture was stirred at room temperature for 14 hours. The solvent was evaporated away under reduced pressure. Isopropanol (4 ml) was added to the obtained solid, and the mixture was stirred at room temperature for 10 minutes. The crystal was collected by filtration, and was dried under reduced pressure to obtain the title compound as a white solid (0.03 g, yield: 28%).

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customThe solvent was evaporated away under reduced pressure
  2. additionIsopropanol (4 ml) was added to the obtained solid
  3. stirringthe mixture was stirred at room temperature for 10 minutes
  4. filtrationThe crystal was collected by filtration
  5. customwas dried under reduced pressure

出典と根拠

ORDレコード
ord-8b511f8a9d4d4523bfcbe6b7b9e1f77e
出典データセット
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07834190B2

反応ノート

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