関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Nitrogen | HCID 947 | — |
| 反応物 | Potassium Phosphate, Tribasic | HCID 62657 | — |
| 反応物 | Formamidine acetate | HCID 160693 | — |
| 反応物 | 1-Amino-4-bromo-1H-pyrrole-2-carbonitrile hydrochloride | HCID 66641268 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 6-Bromopyrrolo[2,1-F][1,2,4]triazin-4-amine | HCID 57955201 | 75.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08829185B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-b855cc33a47c4702bcdf8e99551d67bd |
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| 出典メモ | uspto-grants-2014_09 |
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