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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 409653생성일: 2026년 10월 24일

Phosgene → HCID 23630278, 화합물

https://huagongshe.com/ko/reaction/409653

반응식

참여 물질

역할이름HCID투입량
반응물PhosgeneHCID 6371—
반응물IsocyanateHCID 105034—
반응물Sodium BicarbonateHCID 516892—
반응물2,6-Dichloro-3,5-dimethoxyanilineHCID 59486253—
반응물N-[4-(2-morpholin-4-yl-ethoxy)-phenyl]-pyrimidine-4,6-diamineHCID 59864576—
용매DichloromethaneHCID 6344—
용매N-methyl-2-pyrrolidoneHCID 13387—
용매1,4-DioxaneHCID 31275—
생성물HCID 23630278HCID 23630278—

반응 단계

Phosgene (20% in toluene, 0.8 mL, 1.58 mmol, 2.4 equiv) is added to a solution of 2,6-dichloro-3,5-dimethoxyaniline (175 mg, 0.79 mmol, 1.2 equiv) in dioxane (2.5 mL), under an argon atmosphere. The mixture is heated to reflux, stirred for 1 h, allowed to cool to RT, and concentrated in vacuo. The resulting isocyanate is added to a solution of N-[4-(2-morpholin-4-yl-ethoxy)-phenyl]-pyrimidine-4,6-diamine (208.5 mg, 0.66 mmol) in NMP (2 mL), at 75° C. and under an argon atmosphere. The reaction mixture is stirred at 75° C. for 2 h, allowed to cool to RT, and is then diluted with DCM and a saturated aqueous solution of NaHCO3. The aqueous layer is separated and extracted with DCM. The organic phase is washed with brine, dried (Na2SO4), filtered and concentrated. Purification of the crude product by silica gel column chromatography (DCM/MeOH+1% NH3aq, 96:4), followed by trituration of the resulting material in MeOH, affords the title compound as a white solid: ESI-MS: 562.9/564.9 [MH]+; tR=2.99 min (purity: 100%, system 1); TLC: Rf=0.36 (DCM/MeOH+1% NH3aq, 93:7).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08759517B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-043a0c6a124540bdb2566f4e5faa3739
출처 메모uspto-grants-2014_06