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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 920272생성일: 2026년 10월 26일

Triphenylphosphine → (R)-N-(2,4-Dimethoxybenzyl)-3-(3-hydroxy-1-phenylpropyl)-2-oxo-N-(1,2,4-thiadiazol-5-yl)-2,3-dihydrobenzo[d]oxazole-6-sulfonamide

https://huagongshe.com/reaction/920272

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참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Diethyl azodicarboxylateHCID 5462977—
반응물(1S)-1-phenylpropane-1,3-diolHCID 6950537—
반응물N-(2,4-dimethoxybenzyl)-2-oxo-N-(1,2,4-thiadiazol-5-yl)-2,3-dihydrobenzo[d]oxazole-6-sulfonamideHCID 89526027—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
용매Sodium BicarbonateHCID 516892—
생성물(R)-N-(2,4-Dimethoxybenzyl)-3-(3-hydroxy-1-phenylpropyl)-2-oxo-N-(1,2,4-thiadiazol-5-yl)-2,3-dihydrobenzo[d]oxazole-6-sulfonamideHCID 117629301—

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온도0 °C

반응 단계

Accordingly, the compound of Formula 37-1 (N-(2,4-dimethoxybenzyl)-3-[(1R)-3-hydroxy-1-phenylpropyl]-2-oxo-N-(1,2,4-thiadiazol-5-yl)-2,3-dihydro-1,3-benzoxazole-6-sulfonamide) was prepared from a solution provided by dissolving 200 mg of the compound of Formula 1-5 (0.429 mmol, prepared as described above) and (S)-1-phenylpropane-1,3-diol (65.3 mg, 0.429 mmol) (0.429 mmol) in 2 mL of THF. This solution was cooled to 0° C. and treated with triphenylphosphine (0.225 g, 0.858 mmol) followed by DEAD (0.136 mL, 0.858 mmol). After stirring at 0° C. for 120 min, the reaction mixture was diluted with EtOAc (50 mL) and saturated sodium bicarbonate (5 mL). The organic layer was washed with brine (10 mL), dried over sodium sulfate, filtered, and concentrated in vacuo. Purification by normal phase chromatography (10-80% EtOAc in hexane) yielded the compound of Formula 37-1 as a yellow oil which was used as isolated.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09273040B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-14c7da05a8ef4826adb0e80b937486a6
출처 메모uspto-grants-2016_03