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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16014생성일: 2026년 10월 23일

Sodium hydride → HCID 59341794, 화합물

https://huagongshe.com/ko/reaction/16014

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물HCID 17859945HCID 17859945—
반응물(R)-tert-butyl 1-(3-(quinolin-6-ylmethyl)-3H-[1,2,3]triazolo[4,5-b]pyrazin-5-yl)pyrrolidin-3-ylcarbamateHCID 59341797—
용매DimethylformamideHCID 6228—
생성물HCID 59341794HCID 593417940.6%

반응 단계

To a solution of tert-butyl {(3R)-1-[1-(quinolin-6-ylmethyl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-6-yl]pyrrolidin-3-yl}carbamate (300 mg, 0.672 mmol) in anhydrous DMF (2.0 ml) was added 95% NaH (25.4 mg, 1.01 mmol). After stirring at R.T. for 10 mins, to the reaction mixture was added iodoethanol (288.9 mg, 1.68 mmol). After stirring at 70° C. for 16 h, to the reaction mixture was added iodoethanol (288.9 mg, 1.68 mmol). After stirring at 90° C. for 7 h, 105° C. for 32 h, the reaction mixture was quenched with water and filtered. The eluent was extracted with 2:1 EtOAc:toluene (2×30 ml). The organic layer was dried with K2CO3, filtered and concentrated. The resulting residue was dissolved in CH2Cl2 (10 ml) and TFA (0.5 ml) and MeOH (1 pipet drop) were added. After stirring at R.T for 16 h, the reaction mixture was concentrated. The resulting residue was purified via reversed phase column eluted with 0.1% TFA CAN: water to give the desired product (1.6 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732604B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-c6f2b30405dc4efca0b99cb12c36ac12
출처 메모uspto-grants-2010_06