Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1166생성일: 2026년 10월 23일
2,4-Diamino-6-chloropyrimidine → 6-Chloro-5-[(e)-(4-chlorophenyl)diazenyl]pyrimidine-2,4-diamine
https://huagongshe.com/ko/reaction/1166
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2,4-Diamino-6-chloropyrimidine | HCID 67432 | — |
| 반응물 | Sodium Acetate | HCID 517045 | — |
| 반응물 | Benzenediazonium, 4-chloro-, chloride | HCID 11819533 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 6-Chloro-5-[(e)-(4-chlorophenyl)diazenyl]pyrimidine-2,4-diamine | HCID 267764 | 41.4% |
반응 단계
To a suspension of 4-chloro-2,6-diaminopyrimidine (21.68 g, 0.150 mol) in water (750 ml) and acetic acid (750 ml) was added sodium acetate (300 g). Solution occurred after stirring for 20 minutes, and then the solution of 4-chlorobenzenediazonium chloride (0.166 mol) was added with cooling over 30 minutes at a rate that kept the reaction at 18°. The reaction was stirred overnight at room temperature, and the orange crystals were filtered, washed with water (4×400 ml), and dried in vacuo to give 17.6 g of 6-chloro-5-[(4-chlorophenyl)azo]-2,4-pyrimidinediamine. The mother liquors were cooled to 5° for 20 hours, and the crystals were collected and dried in vacuo to give 6.94 g of additional 6-chloro-5-[(4-chlorophenyl)azo]-2,4-pyrimidineadiamine.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05723609 |
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| 출처 데이터셋 | uspto-grants-1998_03 |
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| ORD ID | ord-db70288e9ca54cb89358931186bc5974 |
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| 출처 메모 | uspto-grants-1998_03 |
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