Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1038741생성일: 2026년 10월 25일
Sodium Bicarbonate → 3-(2,6-Dichloro-3,5-dimethoxy-phenyl)-1-methyl-1-{4-[4-(4-methyl-piperazin-1-yl)-phenylamino]-[1,3,5]triazin-2-yl}-urea
https://huagongshe.com/reaction/1038741
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | HCID 66669974 | HCID 66669974 | — |
| 반응물 | 2,6-Dichloro-3,5-dimethoxyphenyl isocyanate | HCID 86086993 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 3-(2,6-Dichloro-3,5-dimethoxy-phenyl)-1-methyl-1-{4-[4-(4-methyl-piperazin-1-yl)-phenylamino]-[1,3,5]triazin-2-yl}-urea | HCID 57710293 | — |
반응 단계
To a solution of 2,6-dichloro-3,5-dimethoxy-aniline (124 mg, 0.56 mmol; Preparation 2) in 2 ml of dioxane under a nitrogene atmosphere, phosgene (0.52 ml 20% in toluene, 0.98 mmol) is added. The mixture is stirred for 70 min at 100° C., cooled to RT and concentrated in vacuo, yielding 2,6-dichloro-3,5-dimethoxyphenylisocyanate. The resulting solid is added portion-wise to a boiling solution of N-methyl-N′-[4-(4-methyl-piperazin-1-yl)-phenyl]-[1,3,5]triazine-2,4-diamine (140 mg, 0.47 mmol) in 8 ml of toluene during 20 min. After 3 h, another 2 eq of 2,6-dichloro-3,5-dimethoxyphenylisocyanate are added and stirring is continued for totally 5 h. Then the reaction mixture is diluted with DCM and a saturated aqueous solution of NaHCO3. The aqueous layer is separated and extracted twice with DCM. The organic phases are washed with water and brine, dried (Na2SO4) and concentrated. Column chromatography (SiO2; DCM/MeOH/NH3aq, 97:3:0.2) gives the title compound: ESI-MS: 547/549 [MH]+; tR=3.5 min (purity: 100%, gradient J); TLC: Rf=0.40 (DCM/MeOH+1% NH3aq, 95:5).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08552002B2 |
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| 출처 데이터셋 | uspto-grants-2013_10 |
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| ORD ID | ord-d69878926ac6422b822b31e83fa3064e |
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| 출처 메모 | uspto-grants-2013_10 |
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