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HRID 1874473作成日:2026年10月26日

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

https://huagongshe.com/reaction/1874473

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-yloxy)phenylcarbamateHCID 57749334—
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]phenyl}carbamateHCID 5774927994%

反応手順

In the same manner as in Example 17-1 and using tert-butyl {3-[(6-aminopyridin-3-yl)oxy]phenyl}carbamate (15.0 g, 49.8 mmol), ethyl isothiocyanatoformate (7.18 g, 54.8 mmol), DMSO (50 mL), hydroxylammonium chloride (11.8 g, 170 mmol), N,N-diisopropylethylamine (21.2 mL, 122 mmol), ethanol (70 mL) and methanol (70 mL) as starting materials, the title compound (10.5 g, 94%) 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-67168c839fcc4a498f73b6428604e2d4
出典メモuspto-grants-2012_11