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HRID 1424916作成日:2026年10月25日

1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → tert-Butyl cis(+/-)-4-{[(4-chloro-5-methyl-1H-imidazol-2-yl)carbonyl]amino}-3-ethoxypiperidine-1-carboxylate

https://huagongshe.com/reaction/1424916

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物4-chloro-5-methyl-1H-imidazole-2-carboxylic acidHCID 14474277—
反応物Tert-butyl cis(+/-)-4-amino-3-ethoxypiperidine-1-carboxylateHCID 86648467—
触媒4-(Dimethylamino)pyridineHCID 14284—
生成物tert-Butyl cis(+/-)-4-{[(4-chloro-5-methyl-1H-imidazol-2-yl)carbonyl]amino}-3-ethoxypiperidine-1-carboxylateHCID 8664846643%

反応手順

The same operation as in Example (1g) was performed using tert-butyl cis(±)-4-amino-3-ethoxypiperidine-1-carboxylate obtained in Example (18a) (0.34 g, 1.37 mmol), 4-chloro-5-methyl-1H-imidazole-2-carboxylic acid obtained by the method described in Example (5c) (0.16 g, 0.91 mmol), WSC hydrochloride (1.18 g, 6.15 mmol) and DMAP (0.12 g, 0.94 mmol), to obtain 0.23 g of the title compound as a pale yellow solid (43%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08927588B2
出典データセットuspto-grants-2015_01
ORD IDord-64627184f1df4c649a307fe26ee7b21e
出典メモuspto-grants-2015_01