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HRID 1721444作成日:2026年10月27日

1(2H)-Isoquinolinone → 1,2,3,4-Tetrahydro-1-naphthalenecarboxamide

https://huagongshe.com/reaction/1721444

反応式

関与物質

役割名称HCID仕込み量
反応物1(2H)-IsoquinolinoneHCID 10284—
反応物3-OctanamineHCID 547362—
生成物1,2,3,4-Tetrahydro-1-naphthalenecarboxamideHCID 272042—

反応手順

A preferred process for preparing 2-(1-azabicyclo 2.2.2!oct-3-yl)-2,3,3a,4,5,6-hexahydro-1H-benz de!isoquinolin-1-one is that in which L is chloro and the 1-azabicyclo 2.2.2!oct-3-ylamine is (S)-1-azabicyclo 2.2.2!oct-3-ylamine and is reacted with the compound of Formula 5 to give N-(1-azabicyclo 2.2.2!oct-3S-yl)-1,2,3,4-tetrahydronaphthalen-1-ylcarboxamide; and preferably wherein the N-(1-azabicyclo 2.2.2!oct-3S-yl)-1,2,3,4-tetrahydronaphthalen-1-ylcarboxamide is then reduced as N-(1-azabicyclo 2.2.2!oct-3S-yl)-1,2,3,4-tetrahydronaphthalen-1S-ylcarboxamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05510486
出典データセットuspto-grants-1996_04
ORD IDord-37cc6dfb20b94cda976dde7e2b264d52
出典メモuspto-grants-1996_04