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HRID 1874374作成日:2026年10月27日

Ethyl isothiocyanatoformate → Ethyl {[(5-{3-[(tert-butoxycarbonyl)amino]-4-chlorophenoxy}pyridin-2-yl)amino]carbonothioyl}carbamate

https://huagongshe.com/reaction/1874374

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl isothiocyanatoformateHCID 85320—
反応物Tert-butyl {5-[(6-aminopyridin-3-yl)oxy]-2-chlorophenyl}carbamateHCID 57749356—
溶媒Dimethyl SulfoxideHCID 679—
生成物Ethyl {[(5-{3-[(tert-butoxycarbonyl)amino]-4-chlorophenoxy}pyridin-2-yl)amino]carbonothioyl}carbamateHCID 5774919697%

反応手順

In the same manner as in Reference Example 30 and using tert-butyl {5-[(6-aminopyridin-3-yl)oxy]-2-chlorophenyl}carbamate (10.8 g, 32.3 mmol), ethyl isothiocyanatoformate (4.60 mL, 38.9 mmol) and DMSO (60 mL) as starting materials, the title compound (14.6 g, 97%) was obtained as a pale-yellow oil.

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-c2f8746ad1974d088988415eca8f1753
出典メモuspto-grants-2012_11