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HRID 733215作成日:2026年10月25日

Carbamimidoylazanium Chloride → HCID 178462846、化合物

https://huagongshe.com/reaction/733215

反応式

関与物質

役割名称HCID仕込み量
反応物Carbamimidoylazanium ChlorideHCID 5460839—
反応物Potassium tert-butoxideHCID 23665647—
反応物ethyl (2-ethyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)acetateHCID 86591360—
溶媒WaterHCID 962—
生成物HCID 178462846HCID 17846284628%

反応条件

温度20 °C

反応手順

N-[(2-Ethyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)acetyl]guanidine is prepared as described in Example 1, starting with 4.3 g of potassium tert-butoxide, 3.7 g of guanidinium chloride and 1.9 g of ethyl (2-ethyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)acetate. The reaction mixture is stirred at a temperature in the region of 20° C. for 20 hours, followed by addition of 60 cm3 of water. The aqueous phase is extracted with 3 times 50 cm3 of ethyl acetate and is then concentrated to dryness under reduced pressure (0.6 kPa) at a temperature in the region of 45° C. The residue is taken up in water, triturated and filtered. The solid is taken up in methanol and the solvent is then evaporated to dryness under reduced pressure (0.6 kPa) at a temperature in the region of 45° C. 0.56 g of N-[(2-ethyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl)acetyl]-guanidine is thus obtained in the form of an off-white solid melting at 223° C. Mass spectrum EI: m/e 260 (M+), m/e 173, m/e 160, m/e 132.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07589117B2
出典データセットuspto-grants-2009_09
ORD IDord-4dc12b006aff4a4b9c25c9da79083658
出典メモuspto-grants-2009_09