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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1725343생성일: 2026년 10월 27일

Methanol → (R)-3-{3-[(benzo[1,2,5]thiadiazol-5-ylmethyl)-amino]-propyl}-5-(6-methoxyquinolin-4-yl)-oxazolidin-2-one

https://huagongshe.com/reaction/1725343

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물2,1,3-Benzothiadiazole-5-carbaldehydeHCID 2776290—
반응물Sodium borohydrideHCID 4311764—
반응물(R)-3-(3-amino-propyl)-5-(6-methoxy-quinolin-4-yl)-oxazolidin-2-oneHCID 68839629—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물(R)-3-{3-[(benzo[1,2,5]thiadiazol-5-ylmethyl)-amino]-propyl}-5-(6-methoxyquinolin-4-yl)-oxazolidin-2-oneHCID 1000385766.7%

반응 단계

A mixture of (R)-3-(3-amino-propyl)-5-(6-methoxy-quinolin-4-yl)-oxazolidin-2-one (0.15 g, 0.5 mmol), benzo[1,2,5]thiadiazole-5-carbaldehyde (92 mg, 0.56 mmol), methanol (0.5 ml), methylene chloride (1.8 ml), 3 Å dry molecular sieve (1 g) was stirred at room temperature for 16 hours. Sodium borohydride (28 mg, 0.76 mmol) was added and the mixture was stirred for 3 hours. After concentration of the solvent the residue was dissolved in ethyl acetate and the organic phase was washed with water, dried over magnesium sulfate and concentrated. The residue was chromatographed on silicagel eluting with methylene chloride-methanol (99-1 first, then 90-10) to give (R)-3-{3-[(benzo[1,2,5]thiadiazol-5-ylmethyl)-amino]-propyl}-5-(6-methoxyquinolin-4-yl)-oxazolidin-2-one (150 mg, 59%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07491714B2
출처 데이터셋uspto-grants-2009_02
ORD IDord-d65bf6b1fa814a48a53b655c4022039c
출처 메모uspto-grants-2009_02