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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 380470생성일: 2026년 10월 27일

Triethylamine → 1-(7-Indolylcarbonyl)-3-(RS)-(4-phenylpiperidinylmethyl)-4-(RS)-(3-thienyl)pyrrolidine

https://huagongshe.com/reaction/380470

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1H-Indole-7-carboxylic acidHCID 74281—
반응물Bis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 152842—
반응물3-(SR)-(4-phenyl piperidinylmethyl)-4-(RS)-(3-thienyl)pyrrolidineHCID 20694483—
용매DichloromethaneHCID 6344—
생성물1-(7-Indolylcarbonyl)-3-(RS)-(4-phenylpiperidinylmethyl)-4-(RS)-(3-thienyl)pyrrolidineHCID 18364772—

반응 단계

To a solution of 0.022 g (0.067 mmol) of 3-(SR)-(4-phenyl piperidinylmethyl)-4-(RS)-(3-thienyl)pyrrolidine and 0.016 g (0.1 mmol) of indole-7-carboxylic acid in 2 mL of CH2Cl2 and 0.037 mL (0.27 mmol) of triethylamine was added 0.022 g (0.087 mL) of BOP-Cl [Bis-(2-oxo-3-oxazolidinyl)phosphinic chloride] and the reaction mixture was stirred at rt for 5 h. The reaction mixture concentrated and purified by chomatography (silica, acetone: hexanes, 1:3 to 1:2) to give the title compound. 1H NMR (CDCl3) δ; 10.02 (bs, 1H), 7.79 (bs, 1H), 7.02-7.53 (m, 11H), 6.62 (bs, 1H), 4.15-4.19 (m, 2H); Mass Spectrum (CI) m/e=482 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06303593B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-0ab2bd26f98c4fea91a9edbd45f75696
출처 메모uspto-grants-2001_10