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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38454생성일: 2026년 10월 25일

Sodium hydride → 5-(1-Benzyloxy-7-chloro-isoquinolin-6-yloxy)-adamantan-2-ylamine

https://huagongshe.com/reaction/38454

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물4-Aminoadamantan-1-olHCID 2857447—
반응물1-Benzyloxy-7-chloro-6-fluoro-isoquinolineHCID 59818252—
용매DimethylacetamideHCID 31374—
생성물5-(1-Benzyloxy-7-chloro-isoquinolin-6-yloxy)-adamantan-2-ylamineHCID 5838092031.2%

반응 단계

To a suspension of sodium hydride (60% in mineral oil, 417 mg, 10.4 mmol, 3 eq.) in dimethyl acetamide (7 mL) was added a solution of 4-amino-adamantan-1-ol (640 mg, 3.82 mmol, 1.1 eq.) in dimethyl acetamide (7 mL). After stirring for 60 min at room temperature, a solution of 1-benzyloxy-7-chloro-6-fluoro-isoquinoline (1, 1.0 g, 3.48 mmol) in dimethyl acetamide (7 mL) was added and stirring was continued at room temperature until the reaction went to completion. The reaction was quenched by addition of water (15 mL) and the reaction mixture was extracted twice with a mixture of dichloromethane and 2-propanol (3:1). The combined organic layers were evaporated, water was added and the mixture was subjected to lyophilization to remove remainders of dimethyl acetamide. The obtained crude product was purified by flash chromatography (SiO2, 0%→30% methanol in dichloromethane) to yield 473 mg of the title compound as diastereomeric mixture. Rt=1.35 min, 1.55 min (Method 3). Detected mass: 435.2 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524737B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-dc8ea993b9fc424f865103a1858c2ebc
출처 메모uspto-grants-2013_09