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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 264674생성일: 2026년 10월 24일

3,5-Dihydroxybenzoic Acid → (2R*,4S*)-2-benzyl-1-(3,5-dihydroxybenzoyl)-N-(4-quinolylmethyl)-N-trifluoroacetyl-4-piperidinamine

https://huagongshe.com/ko/reaction/264674

반응식

참여 물질

역할이름HCID투입량
반응물3,5-Dihydroxybenzoic AcidHCID 7424—
반응물TriethylamineHCID 8471—
반응물Bis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 152842—
반응물(2R*,4S*)-2-Benzyl-N-(4-quinolylmethyl)-N-trifluoroacetyl-4-piperidinamineHCID 57202094—
생성물(2R*,4S*)-2-benzyl-1-(3,5-dihydroxybenzoyl)-N-(4-quinolylmethyl)-N-trifluoroacetyl-4-piperidinamineHCID 5697689438%

반응 단계

200 mg (0.467 mmol) of (2R*,4S*)-2-benzyl-N-(4-quinolylmethyl)-N-trifluoroacetyl-4-piperidinamine are reacted in analogy to Example 4a with 87 mg (0.562 mmol) of 3,5-dihydroxybenzoic acid, 143 mg (0.561 mmol)of bis-(2-oxo-3-oxazolidinyl)phosphinic chloride and 144 μl (1.03 mmol) of triethylamine. The title compound (99 mg, 38%) is obtained as white foam. TLC: methylene chloride/methanol/conc. ammonia (700:50:1) Rf =0.41, FD-MS: M+ =563.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05646144
출처 데이터셋uspto-grants-1997_07
ORD IDord-34d93cde0e5d4f3d9fd907f5f45f778c
출처 메모uspto-grants-1997_07