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HRID 1874429作成日:2026年10月27日

Hydroxylamine HCl → Tert-butyl {3-[(2-amino[1,2,4]triazolo[1,5-a]pyridin-6-yl)oxy]-4-methylphenyl}carbamate

https://huagongshe.com/reaction/1874429

反応式

関与物質

役割名称HCID仕込み量
反応物Hydroxylamine HClHCID 21645—
反応物DiisopropylethylamineHCID 81531—
反応物Ethyl isothiocyanatoformateHCID 85320—
反応物Tert-butyl {3-[(6-aminopyridin-3-yl)oxy]-4-methylphenyl}carbamateHCID 57749176—
溶媒Dimethyl SulfoxideHCID 679—
溶媒EthanolHCID 702—
溶媒MethanolHCID 887—
生成物Tert-butyl {3-[(2-amino[1,2,4]triazolo[1,5-a]pyridin-6-yl)oxy]-4-methylphenyl}carbamateHCID 5774939187%

反応手順

In the same manner as in Example 17-1 and using tert-butyl {3-[(6-aminopyridin-3-yl)oxy]-4-methylphenyl}carbamate (1.69 g, 5.35 mmol), DMSO (5 mL), ethyl isothiocyanatoformate (843 mg, 6.42 mmol), ethanol (20 mL), methanol (20 mL), hydroxylammonium chloride (2.43 g, 35.0 mmol) and N,N-diisopropylethylamine (4.35 mL, 25.0 mmol) as starting materials, the title compound (1.55 g, 87%) was obtained as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08304557B2
出典データセットuspto-grants-2012_11
ORD IDord-4db9f563c2f542eb90a1e5ba9c8f4e56
出典メモuspto-grants-2012_11