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HRID 442124作成日:2026年10月25日

5,6,7-Trimethoxy-1,2,3,4-tetrahydroisoquinoline → 4-Amino-6,7,8-trimethoxy-2-(5,6,7-trimethoxy-1,2,3,4-tetrahydroisoquinolin-2-yl)quinazoline

https://huagongshe.com/reaction/442124

反応式

関与物質

役割名称HCID仕込み量
反応物5,6,7-Trimethoxy-1,2,3,4-tetrahydroisoquinolineHCID 270529—
反応物2-Chloro-6,7,8-trimethoxyquinazolin-4-amineHCID 3015804—
生成物4-Amino-6,7,8-trimethoxy-2-(5,6,7-trimethoxy-1,2,3,4-tetrahydroisoquinolin-2-yl)quinazolineHCID 21416703—

反応手順

The procedure described in Example 1 was followed to prepare the above compound, starting from 4-amino-2-chloro-6,7,8-trimethoxyquinazoline and using 5,6,7-trimethoxy-1,2,3,4-tetrahydroisoquinoline as the regent of choice on the same molar basis as before. In this particular instance, the final product was obtained as the free base compound, m.p. 193°-195° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04044136
出典データセットuspto-grants-1977_08
ORD IDord-8bd2c6be9fcd412591a7f0c51c5ad37e
出典メモuspto-grants-1977_08