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HRID 456133作成日:2026年10月26日

N,1-Dimethylhydrazine-1-carboxamide → 1,3-dimethyl-1-[(E)-1-[3-(quinolin-6-ylmethyl)triazolo[4,5-b]pyrazin-5-yl]ethylideneamino]urea

https://huagongshe.com/reaction/456133

反応式

関与物質

役割名称HCID仕込み量
反応物N,1-Dimethylhydrazine-1-carboxamideHCID 304021—
反応物1-(1-(Quinolin-6-ylmethyl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-6-yl)ethanoneHCID 59341802—
生成物1,3-dimethyl-1-[(E)-1-[3-(quinolin-6-ylmethyl)triazolo[4,5-b]pyrazin-5-yl]ethylideneamino]ureaHCID 71699919—

反応手順

The title compound was prepared in analogy to the synthesis of example 52 from 1-(1-(quinolin-6-ylmethyl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-6-yl)ethanone and N,1-dimethyl-hydrazinecarboxamide. 1H-NMR (400 MHz, DMSO-d6) δ ppm 9.73 (s, 1H), 8.89 (m, 1H), 8.36 (dd, 1H), 8.03 (s, 1H), 8.00 (d, 1H), 7.53 (dd, 1H), 7.19 (m, 1H), 6.21 (s, 2H), 3.31 (s, 3H), 2.72 (d, 3H), 2.49 (d, 3H). LCMS (method B): [MH]+=390, tR=1.99 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08497368B2
出典データセットuspto-grants-2013_07
ORD IDord-2a9ea274b39a4522b50d812b5d0d152d
出典メモuspto-grants-2013_07