戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 73687作成日:2026年10月23日

Nitrogen → 6-Bromopyrrolo[2,1-F][1,2,4]triazin-4-amine

https://huagongshe.com/ja/reaction/73687

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物Formamidine acetateHCID 160693—
反応物1-Amino-4-bromo-1H-pyrrole-2-carbonitrile hydrochlorideHCID 66641268—
溶媒EthanolHCID 702—
生成物6-Bromopyrrolo[2,1-F][1,2,4]triazin-4-amineHCID 5795520175.8%

反応手順

To a stirred suspension of 1-Amino-4-bromo-1H-pyrrole-2-carbonitrile hydrochloride (17 g, 61.1 mmol) in absolute ethanol (350 mL) was added formamidine acetate (31.8 g, 305 mmol) and potassium phosphate (64.9 g, 305 mol). The suspension was heated for 18 hours @ 78° C. (under N2), then cooled, filtered and concentrated to dryness in vacuo. The residue was mixed with ice water (2 L) and the dark grayish-brown solids were collected by suction filtration. The solids were taken up in refluxing MeOH and treated with decolorizing carbon, then filtered thru Celite and concentrated dryness in vacuo. The solids were taken up in THF:DCE (1:3) and filtered thru a pad of silica. Removal of the solvent in vacuo provided a yellowish-brown solid. This material was recrystallized from THF:hexanes to provide the desired compound as a yellow solid (9.86 g, 75% yield). (81%). 1H-NMR (DMSO): δ 7.85 (bs, 2H), 7.81 (s, 1H), 7.80 (d, 1H, J=2 Hz), 6.96 (d, 1H, J=2 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08829185B2
出典データセットuspto-grants-2014_09
ORD IDord-b855cc33a47c4702bcdf8e99551d67bd
出典メモuspto-grants-2014_09