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Thiophene-3,4-diamine → 2-butyl-1H-thieno[3,4-d]imidazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Thiophene-3,4-diamine | HCID 643216 | — |
| 反応物 | Ethyl pentanimidate hydrochloride | HCID 12283341 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-butyl-1H-thieno[3,4-d]imidazole | HCID 19370634 | 78% |
反応手順
A mixture of 3,4-diaminothiophene (116 mg, 1.01 mmol ) and ethyl valeroimidate hydrochloride (504 mg, 3.05 mmol) in absolute ethanol (20 mL) was heated to reflux for 1 hour, cooled to room temperature and stirred for 15 hours. The mixture was concentrated and purified by flash chromatography (SiO2, 25% EtOAc/hexanes) to give 140 mg (78%) of 2-n-butyl-1H-thieno[3,4-d]imidazole as a tan solid: 1H NMR (300 MHz, CDCl3)δ 6.70 (s, 2H), 2.81 (t, 2H, J=7.5 Hz), 1.88-1.74 (m, 2H), 1.48-1.35 (m, 2H), 0.90 (t, 3H, J=7.2 Hz); FAB-MS: 181 (M+ +1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05389660 |
| 出典データセット | uspto-grants-1995_02 |
| ORD ID | ord-f98a85bc928049fdbbeb847516e9f0b0 |
| 出典メモ | uspto-grants-1995_02 |