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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 73687생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물Formamidine acetateHCID 160693—
반응물1-Amino-4-bromo-1H-pyrrole-2-carbonitrile hydrochlorideHCID 66641268—
용매EthanolHCID 702—
생성물6-Bromopyrrolo[2,1-F][1,2,4]triazin-4-amineHCID 5795520175.8%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829185B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-b855cc33a47c4702bcdf8e99551d67bd
출처 메모uspto-grants-2014_09