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HRID 252978作成日:2026年10月26日
2-Dimethylaminopyridine → (3-methoxy-phenyl)-carbamic acid 3-{4-[N'-(3-methyl-benzylidene)-hydrazino]-6-morpholin-4-yl-pyrimidin-2-yl}-propyl ester
https://huagongshe.com/reaction/252978
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 2-Dimethylaminopyridine | HCID 21885 | — |
| 反応物 | 3-Methoxyphenyl isocyanate | HCID 87843 | — |
| 反応物 | 3-{4-[N'-(3-methyl-benzylidene)-hydrazino]-6-morpholin-4-yl-pyrimidin-2-yl}-propan-1-ol | HCID 66840679 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | (3-methoxy-phenyl)-carbamic acid 3-{4-[N'-(3-methyl-benzylidene)-hydrazino]-6-morpholin-4-yl-pyrimidin-2-yl}-propyl ester | HCID 66841255 | — |
反応手順
S5; 3-{4-[N′-(3-methyl-benzylidene)-hydrazino]-6-morpholin-4-yl-pyrimidin-2-yl}-propan-1-ol (355 mg, 1 mmol) was dissolved in acetonitrile (4 mL). To the mixture was added m-methoxyphenylisocyanate (149 mg., 1 mmol) and a catalytic amount of dimethylaminopyridine. The reaction was stirred at 60° C. for 16 hours. The reaction was then cooled to 4° C., and the precipitate was filtered, washed with acetonitrile (1 mL) and dried to give Compound 1, (3-methoxy-phenyl)-carbamic acid 3-{4-[N′-(3-methyl-benzylidene)-hydrazino]-6-morpholin-4-yl-pyrimidin-2-yl}-propyl ester.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07872005B2 |
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| 出典データセット | uspto-grants-2011_01 |
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| ORD ID | ord-82d6c132e0e44fc6b47f970f7b5632cb |
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| 出典メモ | uspto-grants-2011_01 |
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