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HRID 1040463作成日:2026年10月25日

Ammonia → tert-butyl N-(1-carbamimidoylcyclopropyl)carbamate

https://huagongshe.com/reaction/1040463

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物MethanolHCID 887—
反応物Ammonium ChlorideHCID 25517—
反応物Sodium ethoxideHCID 2723922—
反応物tert-butyl N-(1-cyanocyclopropyl)carbamateHCID 20825555—
溶媒EthanolHCID 702—
生成物tert-butyl N-(1-carbamimidoylcyclopropyl)carbamateHCID 58430989109%

反応手順

(1-Cyano-cyclopropyl)-carbamic acid tert-butyl ester (2.44 g, 13.40 mmol) was dissolved in dry EtOH (33 mL). Sodium ethoxide (21 wt % in EtOH solution, 10.70 mL, 22.80 mmol)) was added and the reaction was stirred for 1 h at room temperature under an atmosphere of dry argon. To the light yellow solution was added solid NH4Cl (2.94 g, 55 mmol) followed by 7 M NH3 in MeOH (8.08 mL, 56.60 mmol). The reaction was capped and allowed to stir for 16 h. The turbid suspension was filtered using MeOH to rinse. The filtrate was concentrated in vacuo and the solid residue was re-suspended in dry EtOH. The solids were filtered off, rinsing with EtOH. The filtrate was concentrated to give 2.91 g of (1-Carbamimidoyl-cyclopropyl)-carbamic acid tert-butyl ester as a light yellow solid. m/z 200.48 [M+1]+

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08552205B2
出典データセットuspto-grants-2013_10
ORD IDord-373987b60a034396b7874d2d38168718
出典メモuspto-grants-2013_10