Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38400생성일: 2026년 10월 24일
Benzenamine hydrochloride (1:1) → 5-(2-Isopropyl-4-methoxy-5-thiazol-4-yl-phenoxy)-pyrimidine-2,4-diamine
https://huagongshe.com/ko/reaction/38400
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzenamine hydrochloride (1:1) | HCID 8870 | — |
| 반응물 | tert-Butoxy bis(dimethylamino)methane | HCID 79885 | — |
| 반응물 | Carbonic acid-guanidine (1:1) | HCID 286947 | — |
| 반응물 | (2-Isopropyl-4-methoxy-5-thiazol-4-yl-phenoxy)-acetonitrile | HCID 59598608 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 생성물 | 5-(2-Isopropyl-4-methoxy-5-thiazol-4-yl-phenoxy)-pyrimidine-2,4-diamine | HCID 59598634 | 68% |
반응 단계
A mixture of (2-Isopropyl-4-methoxy-5-thiazol-4-yl-phenoxy)-acetonitrile (0.27 g, 0.94 mmol) and Brederick's reagent (0.35 g, 2.01 mmol) was heated at 100° C. for 2 hrs. Excess Brederick's reagent was removed under reduced pressure. The residue was dissolved in anhydrous EtOH (10 ml) and aniline HCl (0.38 g, 2.93 mmol) was added. The reaction mixture was heated at 80° C. for 18 hrs and partitioned between EtOAc and water. The combined organic extracts were dried over Na2SO4, filtered and concentrated. Guanidine carbonate (0.27 g, 1.49 mmol) and NMP (10 ml) were added and heated to 120° C. for 10 hrs. The reaction mixture was poured into water and extracted into EtOAc. The combined organic extracts were dried over Na2SO4, filtered and concentrated. Flash chromatography on silica (3% MeOH in methylene chloride with 0.1% NH4OH) gave 5-(2-Isopropyl-4-methoxy-5-thiazol-4-yl-phenoxy)-pyrimidine-2,4-diamine (0.15 g, 68%) as a solid. (M+H)=358.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08524725B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-8c06519b6f364e26b61c9ee879ec780f |
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| 출처 메모 | uspto-grants-2013_09 |
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