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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 264694생성일: 2026년 10월 25일

Triethylamine → (2R*,4S*)-2-benzyl-1-(3,5-dichlorobenzoyl)-N-(2-indolylcarbonyl)-4-piperidinamine

https://huagongshe.com/reaction/264694

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Indole-2-carboxylic acidHCID 72899—
반응물Bis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 152842—
반응물(2R*,4S*)-2-benzyl-1-(3,5-dichlorobenzoyl)-4-piperidinamineHCID 53839030—
생성물(2R*,4S*)-2-benzyl-1-(3,5-dichlorobenzoyl)-N-(2-indolylcarbonyl)-4-piperidinamineHCID 57278312—

반응 단계

200 mg (0.550 mmol) of (2R*,4S*)-2-benzyl-1-(3,5-dichlorobenzoyl)-4-piperidinamine are reacted in analogy to Example 4a with 106 mg (0.661 mmol) of indole-2-carboxylic acid, 168 mg (0.661 mmol) of bis(2-oxo-3-oxazolidinyl)phosphinic chloride and 169 μl (1.21 mmol) of triethylamine. The title compound ##STR87## is obtained (89 mg, 32%) as white crystals with melting point 254° C. TLC:methylene chloride/methanol/cone. ammonia (2000:50:1) Rf =0.56, FD-MS:M+ =505, 507; IR:3430, 3290, 1625 cm-1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05646144
출처 데이터셋uspto-grants-1997_07
ORD IDord-147e3f0a74854dae8442e44ef1feb4cf
출처 메모uspto-grants-1997_07