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5-Amino-4-cyanopyrazole → HCID 178510454、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 5-Amino-4-cyanopyrazole | HCID 85515 | — |
| 反応物 | Methyl 2-[4-(benzyloxy)phenyl]-3-dimethylamino-2-propenoate | HCID 69154646 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | HCID 178510454 | HCID 178510454 | 65% |
反応手順
A solution of 1.21 g (3.9 mmol) of 2-(4-benzyloxy-phenyl)-3-dimethylamino-acrylic acid methyl ester and 0.422 g (3.9 mmol) of 5-amino-1H-pyrazole-4-carbonitrile in 5 mL of acetic acid (HOAc) was heated at reflux overnight, during which time a precipitate formed. The reaction mixture was cooled to rt, diluted with 20% ethyl acetate in hexane solution, and filtered to give 0.86 g (65% over 2 steps) of 6-(4-benzyloxy-phenyl)-7-oxo-4,7-dihydro-pyrazolo[1,5-a]pyrimidine-3-carbonitrile as a tan colored solid as indicated by 1H NMR; LC-MS—calcd for C20H14N4O2 [M++H]+: 343.11, found: 343.1.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07196111B2 |
| 出典データセット | uspto-grants-2007_03 |
| ORD ID | ord-0e85afbb4c4b4fdf8d26dc6496a80b66 |
| 出典メモ | uspto-grants-2007_03 |