Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 243319생성일: 2026년 10월 26일
2-Amino-4-chloropyrimidine → (S)-N4-(1-(1-phenyl-1H-benzo[d]imidazol-2-yl)ethyl)pyrimidine-2,4-diamine
https://huagongshe.com/reaction/243319
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 2-Amino-4-chloropyrimidine | HCID 223332 | — |
| 반응물 | (S)-1-(1-Phenyl-1H-benzo[D]imidazol-2-YL)ethanamine | HCID 68157455 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | (S)-N4-(1-(1-phenyl-1H-benzo[d]imidazol-2-yl)ethyl)pyrimidine-2,4-diamine | HCID 60161632 | 45.9% |
반응 단계
Into a 25-mL round-bottom flask was placed a solution of (S)-1-(1-phenyl-1H-benzo[d]imidazol-2-yl)ethanamine from Example 4 (238 mg, 1.00 mmol, 1.00 equiv) in ethanol (8 mL) and 4-chloropyrimidin-2-amine (130 mg, 0.99 mmol, 0.98 equiv, 98%). The resulting solution was stirred overnight at 100° C. and concentrated under vacuum. The crude product was applied onto a C18 Column (water/acetonitrile) to afford 150 mg (44%) of 145 as a white solid. LC-MS (ES, m/z): 331 [M+H]+ H-NMR (300 MHz, CD3OD, ppm): δ 7.83 (d, 1H), 7.57 (m, 8H), 6.11 (q, 1H), 5.61 (q, 1H), 1.67 (d, 3H)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08653089B2 |
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| 출처 데이터셋 | uspto-grants-2014_02 |
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| ORD ID | ord-38eef9e5d8a54aadabfb54f4e5de317f |
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| 출처 메모 | uspto-grants-2014_02 |
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