関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Chloroform methanol | HCID 21584188 | — |
| 反応物 | HCID 178493670 | HCID 178493670 | — |
| 反応物 | 2-Guanidino-4-(3-aminocyclohexyl)thiazole | HCID 178512612 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | HCID 178512613 | HCID 178512613 | — |
反応手順
To a solution of 1-[3-(2-guanidinothiazol-4-yl)cyclohexylamino]-2-methoxycyclobutene-3,4-dione (0.1 g.) in 15 ml. of methanol/chloroform (50:50 v/v) was added a solution of 2-guanidino-4-(3-aminocyclohexyl)thiazole (0.07 g.) in methanol (3 ml.) and the resulting solution was allowed to stand at room temperature for 6 hours. After heating under reflux for 6 hours, the reaction mixture was concentrated and cooled to give, as a white amorphous solid, 1,2-bis[3-(2-guanidinothiazol-4-yl)cyclohexylamino]cyclobutene-3,4-dione. The carbon-13 magnetic resonance spectrum (δ relative to tetramethylsilane) in d6DMSO included one carbon singlets at 181.9, 175.0 167.0, 156.8, 155.4, 100.3, 52.4 and a series of signals from 52.4 to 24.1 (including resonances attributable to solvent) p.p.m.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04342765 |
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| 出典データセット | uspto-grants-1982_08 |
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| ORD ID | ord-e5d36c8635d848f5afc9e14c4790c06c |
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| 出典メモ | uspto-grants-1982_08 |
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