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HRID 1378380作成日:2026年10月27日

1,2-Dihydro-6,7-dimethoxy-3-nitronaphthalene → trans-1,2,3,4-Tetrahydro-6,7-dimethoxy-1-(4-hydroxymethyl-5-methyl-3-pyridinyl)-2-nitro-naphthalene

https://huagongshe.com/reaction/1378380

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-Dihydro-6,7-dimethoxy-3-nitronaphthaleneHCID 10752220—
反応物(3-Bromo-5-methyl-4-pyridyl)methyl methoxymethyl etherHCID 22911326—
生成物trans-1,2,3,4-Tetrahydro-6,7-dimethoxy-1-(4-hydroxymethyl-5-methyl-3-pyridinyl)-2-nitro-naphthaleneHCID 54195408—

反応手順

The compound of step 14c was condensed with 1,2-dihydro-6,7-dimethoxy-3-nitronaphthalene according to the procedure of Example 13c. The protecting methoxymethyl group was removed from the intermediate by a standard hydrolysis method (HCl, ethanol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05668141
出典データセットuspto-grants-1997_09
ORD IDord-6d128bcaec534abc8e0d097f2016431f
出典メモuspto-grants-1997_09