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HRID 1938552作成日:2026年10月26日

Methanesulfonic Acid → 2-(4-Carboxypiperidino)-4-(3,4-methylenedioxy-benzyl)amino-6-chloroquinazoline methanesulfonate

https://huagongshe.com/reaction/1938552

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfonic AcidHCID 6395—
反応物1-(6-Chloro-4-(3,4-methylenedioxybenzyl)aminoquinazolin-2-yl)piperidine-4-carboxylic acidHCID 5311486—
溶媒EthanolHCID 702—
溶媒TetrahydrofuranHCID 8028—
生成物2-(4-Carboxypiperidino)-4-(3,4-methylenedioxy-benzyl)amino-6-chloroquinazoline methanesulfonateHCID 2118403290.7%

反応手順

2.00 g (4.54 mmol) of the 2-(4-carboxypiperidino)-4-(3,4-methylenedioxybenzylamino)-6-chloroquinazoline prepared in Example 222 was dissolved in a mixture comprising 25 ml of tetrahydrofuran and 25 ml of ethanol under heating, followed by the dropwise addition of 0.31 ml (4.78 mmol) of methanesulfonic acid. The obtained mixture was cooled by allowing to stand to precipitate crystals. The crystals were recovered by filtration, washed with tetrahydrofuran, and air-dried to give 2.21 g of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05693652
出典データセットuspto-grants-1997_12
ORD IDord-b81665562bfd469bb00e23b65d005a11
出典メモuspto-grants-1997_12