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HRID 989599作成日:2026年10月26日

2-Nitrophenylacetonitrile → 2-(4,6-Dimethoxypyrimidine-2-yl)-2-(2-nitrophenyl)acetonitrile

https://huagongshe.com/reaction/989599

反応式

関与物質

役割名称HCID仕込み量
反応物2-NitrophenylacetonitrileHCID 11888—
反応物2-(4,6-Dimethoxypyrimidine-2-yl)acetonitrileHCID 14580674—
生成物2-(4,6-Dimethoxypyrimidine-2-yl)-2-(2-nitrophenyl)acetonitrileHCID 18417990—

反応手順

The compound of the general formula (II) can be produced, for example, as follows. A 2-nitrophenylacetonitrile derivative is reacted with a 2-halogeno- or alkylsulfonyl-4,6-dimethoxypyrimidine in the presence of a base, or a 2-halogeno-nitrobenzene derivative is reacted with 2-(4,6-dimethoxypyrimidine-2-yl)acetonitrile in the presence of a base, to obtain 2-(4,6-dimethoxypyrimidine-2-yl)-2-(2-nitrophenyl)acetonitrile (IV). The compound (IV) is subjected to oxidative decyanation to obtain a compound of the general formula (V). The nitro group of the compound (V) is reduced to convert it into an amino group to obtain a compound of the general formula (VI). The carbonyl group of the compound (VI) is reduced to a hydroxymethyl group to obtain a compound of the general formula (II).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06458748B1
出典データセットuspto-grants-2002_10
ORD IDord-7238791e9d514707962d083a4d051e8a
出典メモuspto-grants-2002_10