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2-Amino-6-chloropyridine-3,5-dicarbonitrile → 2-Aminopyridine-3,5-dicarbonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Amino-6-chloropyridine-3,5-dicarbonitrile | HCID 295901 | — |
| 溶媒 | Cyclohexane ethylacetate | HCID 21867204 | — |
| 生成物 | 2-Aminopyridine-3,5-dicarbonitrile | HCID 295912 | 73% |
反応手順
2-Amino-3,5-dicyanopyridine (5) was prepared from 3 using the procedure described below for the preparation of 5 except that 5 was recrystallised from MeCN [methyl cyanide; acetonitrile) (instead of EtOH). The yield was 73% (7.00 g from 12.0 g (67.2 mmol) of 3] of product homogeneous on TLC (cyclohexane-EtOAc, 1:1); mp 220° C. dec; 1H NMR (Me2SO-d6) δ7.90 (s, NH2), 8.40 and 8.58 (two d, 4-H and 6H, J=2 Hz).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04725687 |
| 出典データセット | uspto-grants-1988_02 |
| ORD ID | ord-f59a2889ea174bf0ac3472c52a9f95d2 |
| 出典メモ | uspto-grants-1988_02 |