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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43448생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/43448

반응식

참여 물질

역할이름HCID투입량
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물4-chloro-5-methyl-1H-imidazole-2-carboxylic acidHCID 14474277—
반응물Tert-butyl cis(+/-)-4-amino-3-propoxypiperidine-1-carboxylateHCID 67548306—
촉매4-(Dimethylamino)pyridineHCID 14284—
생성물tert-Butyl cis(+/-)-4-{[(4-chloro-5-methyl-1H-imidazol-2-yl)carbonyl]amino}-3-propoxypiperidine-1-carboxylateHCID 8664846860%

반응 단계

The same operation as in Example (1g) was performed using tert-butyl cis(±)-4-amino-3-propoxypiperidine-1-carboxylate obtained in Example (20a) (0.22 g, 0.85 mmol), 4-chloro-5-methyl-1H-imidazole-2-carboxylic acid obtained by the method described in Example (5c) (0.11 g, 0.64 mmol), WSC hydrochloride (0.63 g, 3.28 mmol) and DMAP (84 mg, 0.69 mmol), to obtain 0.15 g of the title compound as a pale yellow solid (60%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536197B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-bec2c133dc154395b3cc2cbb68146849
출처 메모uspto-grants-2013_09