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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 651638생성일: 2026년 10월 26일

Triethylamine → 5-Pyridin-3-yl-thiophene-2-sulfonic acid-[1-(1-chloro-isoquinolin-7-ylmethyl)-2-oxopyrrolidin-3-(S)-yl]-amide

https://huagongshe.com/reaction/651638

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물5-Pyridin-3-yl-thiophene-2-sulfonyl chlorideHCID 10658976—
반응물3-(S)-Amino-1-(1-chloro-isoquinolin-7-ylmethyl)-pyrrolidin-2-one hydrochlorideHCID 20680708—
용매AcetonitrileHCID 6342—
생성물5-Pyridin-3-yl-thiophene-2-sulfonic acid-[1-(1-chloro-isoquinolin-7-ylmethyl)-2-oxopyrrolidin-3-(S)-yl]-amideHCID 2068073563.4%

반응 단계

Triethylamine (0.35 mL, 2.5 mmol) is added dropwise to a solution of 5-pyridin-3-yl-thiophene-2-sulfonyl chloride (0.22 g, 0.85 mmol) and 3-(S)-amino-1-(1-chloro-isoquinolin-7-ylmethyl)-pyrrolidin-2-one hydrochloride (0.22 g, 0.71 mmol) in CH3CN (5 mL). The suspension is stirred at room temperature overnight then concentrated to dryness. The residue is diluted with methylene chloride and washed with saturated NaHCO3 solution and brine. The organic layer is dried over MgSO4, filtered, concentrated, and then purified by column chromatography eluting with a gradient of 1% MeOH/CH2Cl2 to 5% MeOH/CH2Cl2 to give the product (0.23 g, 0.45 mmol) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06281227B1
출처 데이터셋uspto-grants-2001_08
ORD IDord-cc7df4c7111441acb5f91233ac9d297f
출처 메모uspto-grants-2001_08