関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonia acetate | HCID 12432 | — |
| 反応物 | Triethyl orthoacetate | HCID 66221 | — |
| 反応物 | 2-Amino-4,5-dimethyl-thiophene-3-carbonitrile | HCID 290236 | — |
| 生成物 | 2,5,6-Trimethylthieno[2,3-d]pyrimidin-4-amine | HCID 25224341 | 60% |
反応手順
A mixture of 2-amino-4,5-dimethylthiophene-3-carbonitrile (200 mg, 1.32 mmol), ammonia acetate (204 mg, 2.64 mmol), and triethyl orthoacetate (2.0 mL) was stirred in a sealed tube at 120° C. overnight. After the reaction mixture was cooling down to room temperature, the precipitate was collected by filtration, rinsed with EtOAc and dried in the air to give title compound (52 mg, 60%) as a yellow solid. 1H NMR (400 MHz, CDCl3) δ2.41 (s, 3H), 2.45 (s, 3H), 2.56 (s, 3H), 5.28 (bs, 2H). MS 194 (MH+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08541421B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-351ac407a6b3414eafc82a489c82274a |
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| 出典メモ | uspto-grants-2013_09 |
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