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Triethylamine → HCID 178514734、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 4-Isothiocyanatobenzenesulfonamide | HCID 521359 | — |
| 反応物 | HCID 178510988 | HCID 178510988 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | HCID 178514734 | HCID 178514734 | 96% |
反応手順
To a suspension of 4-isothiocyanatobenzenesulfonamide (11 mg, 0.05 mmol) in dry acetonitrile (1 mL) and triethylamine (15 μL, 0.11 mmol) was added tricarbonyl rhenium(I) 6-(bis(pyridin-2-ylmethyl)amino)hexylamine trifluoroacetate (40 mg, 0.48 mmol). The reaction mixture was stirred for 3 h at room temperature. The reaction mixture was concentrated and the resulting solid recrystallized from methanol/water to afford MIP-1140 as an off-white solid (38 mg, 96%). 1H NMR (400 MHz, DMSO-d6) δ 9.83 (br, 1H), 8.80 (d, J=5.4 Hz, 2H), 8.11 (br, 1H), 7.96 (m, 2H), 7.86-7.25 (m, 10H), 4.90 (m, 4H) 3.72 (m, 2H), 3.47 (br, 2H), 1.83 (br, 2H), 1.57 (m, 2H), 1.37 (bm, 8H); (M+H)+ (811).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08877970B2 |
| 出典データセット | uspto-grants-2014_11 |
| ORD ID | ord-08ed7f9128194642b60b3f784d72eb49 |
| 出典メモ | uspto-grants-2014_11 |