Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 605214생성일: 2026년 10월 25일
Ammonium Chloride → {4-[2-Amino-4-(5-chloro-pyridin-2-ylcarbamoyl)-phenoxy]-phenyl}-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/605214
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | {4-[4-(5-Chloro-pyridin-2-ylcarbamoyl)-2-nitro-phenoxy]-phenyl}-carbamic acid tert-butyl ester | HCID 67040773 | — |
| 촉매 | Iron | HCID 23925 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | {4-[2-Amino-4-(5-chloro-pyridin-2-ylcarbamoyl)-phenoxy]-phenyl}-carbamic acid tert-butyl ester | HCID 67040733 | 94.5% |
반응 단계
A suspension of the product of Example 199B (282 mg, 0.5816 mmol), iron powder (200 mg, 3.577 mmol), and ammonium chloride (204 mg, 3.809 mmol) in ethanol (8 mL) and water (4 mL) was heated at 80° C. for 45 minutes. After cooling to room temperature, the mixture was diluted with ethyl acetate (100 mL) and washed with water (2×50 mL) and brine (50 mL). The organic phase was dried over sodium sulfate, filtered and concentrated under vacuum to provide the title compound as a beige solid (250 mg, 94%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07910595B2 |
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| 출처 데이터셋 | uspto-grants-2011_03 |
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| ORD ID | ord-89deecb5399e40a6ba749352df6d4c38 |
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| 출처 메모 | uspto-grants-2011_03 |
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