反応式
C(OC([NH:8][NH:9][C:10]1[CH:15]=[CH:14][C:13]([C:16](=[O:29])[NH:17][CH:18]2[CH2:23][C:22]([CH3:25])([CH3:24])[N:21]([CH3:26])[C:20]([CH3:28])([CH3:27])[CH2:19]2)=[CH:12][CH:11]=1)=O)(C)(C)C>Cl.O1CCOCC1>[NH:9]([C:10]1[CH:15]=[CH:14][C:13]([C:16]([NH:17][CH:18]2[CH2:19][C:20]([CH3:27])([CH3:28])[N:21]([CH3:26])[C:22]([CH3:25])([CH3:24])[CH2:23]2)=[O:29])=[CH:12][CH:11]=1)[NH2:8]参加物
4
実験手順
N′-[4-(1,2,2,6,6-Pentamethyl-piperidin-4-ylcarbamoyl)-phenyl]-hydrazinecarboxylic acid tert-butyl ester was dissolved in 4M HCl in dioxane (30 ml) and left to stir for 1-2 hrs. The solution went quickly from a deep orange colour to a bright orange colour. After 1 hr reaction time, the solvent was removed under vacuum to reveal an orange oil that under a vacuum for several minutes crystallized out to give orange crystals in a sticky orange oil. Yield: 4.68 g, 87%.
後処理
- waitleft
- customAfter 1 hr reaction time
- customthe solvent was removed under vacuum
- customfor several minutes
- customcrystallized out
- customto give orange crystals in a sticky orange oil
出典と根拠
- ORDレコード
- ord-5b77d78ce39a4fd09e6898eed2cf261a
- 出典データセット
- uspto-grants-2012_04
- 特許番号
- US08163757B2
関連ノート
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