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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 394611생성일: 2026년 10월 24일

Triethylamine → Thieno(3,2-B)pyridine-2-sulfonic acid (1-(1-amino-isoquinolin-7-ylmethyl)-2-oxo-pyrroldin-3-YL)-amide

https://huagongshe.com/ko/reaction/394611

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Thieno[3,2-b]pyridine-2-sulfonyl chlorideHCID 18176395—
반응물3-(S)-Amino-1-(1-chloro-isoquinolin-7-ylmethyl)-pyrrolidin-2-one hydrochlorideHCID 20680708—
용매AcetonitrileHCID 6342—
생성물Thieno(3,2-B)pyridine-2-sulfonic acid (1-(1-amino-isoquinolin-7-ylmethyl)-2-oxo-pyrroldin-3-YL)-amideHCID 44548033.3%

반응 단계

To a solution of 3-(S)-amino-1-(1-chloro-isoquinolin-7-ylmethyl)-pyrrolidin-2-one hydrochloride (0.15 g, 0.48 mmol) suspended in CH3CN (2.5 mL) is added triethylamine (0.23 mL, 1.6 mmol) followed by thieno[3,2-b]pyridine-2-sulfonyl chloride (0.14 g, 0.55 mmol). The mixture is stirred overnight, then concentrated. The residue is diluted with CH2Cl2 and washed with saturated NaHCO3 and brine. The organic layer is dried over MgSO4, filtered and concentrated to dryness. The crude product is purified by column chromatography eluting with 5% MeOH/CH2Cl2 to give the title compound (0.076 g, 0.16 mmol) as a light yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06602864B1
출처 데이터셋uspto-grants-2003_08
ORD IDord-49ab99c121e24c79b203a0490626ddbf
출처 메모uspto-grants-2003_08