Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 472543생성일: 2026년 10월 26일
tert-Butyl 4-(3-aminophenyl)piperazine-1-carboxylate → 4-(3-[8-(2-Methoxy-5-trifloromethylphenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-ylamino]-phenyl)-piperazine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/472543
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | tert-Butyl 4-(3-aminophenyl)piperazine-1-carboxylate | HCID 22330182 | — |
| 반응물 | 2-Chloro-8-(2-methoxy-5-trifluoromethyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridine | HCID 67478949 | — |
| 생성물 | 4-(3-[8-(2-Methoxy-5-trifloromethylphenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-ylamino]-phenyl)-piperazine-1-carboxylic acid tert-butyl ester | HCID 67481479 | — |
반응 단계
4-(3-[8-(2-methoxy-5-trifloromethylphenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-ylamino]-phenyl)-piperazine-1-carboxylic acid tert-butyl ester was prepared from 2-chloro-8-(2-methoxy-5-trifluoromethyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridine (0.150 g, 0.5 mmol), and 4-(3-amino-phenyl)piperazine-1-carboxylic acid tert-butyl ester (0.152 g, 0.548 mmol) in a manner analogous to Example 2d. Product was isolated as a foam (0.19 g, 73%). 1H NMR (400 MHz, CDCl3, δ, ppm): 8.47 (d, J=6.1 Hz, 1H), 7.93 (s, 1H), 7.69 (d, J=8.1 Hz, 1H), 7.56 (d, J=6.1 Hz, 1H), 7.46-7.40 (m, 2H), 7.31-7.28 (m, 1H), 7.13 (d, J=8.1 Hz, 1H), 7.00-6.94 (m, 1H), 6.87 (s, 1H), 6.84 (d, J=8.1 Hz, 1H), 3.88 (s, 3H), 2.89-2.75 (m, 2H), 2.73-2.63 (m, 1H), 1.92-1.79 (m, 2H), 1.73-1.63 (m, 4H), 1.52 (s, 9H). MS=568 (MH)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08633173B2 |
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| 출처 데이터셋 | uspto-grants-2014_01 |
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| ORD ID | ord-1847a7e4f33b427f8dafbdffefbde47c |
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| 출처 메모 | uspto-grants-2014_01 |
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