Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4727생성일: 2026년 10월 23일
2-[4-(3-Chloro-propoxy)-phenyl]-imidazo[1,2-a]pyridine → Dibutyl-[3-(4-imidazo[1,2-a]pyridin-2-yl-phenoxy)-propyl]-amine
https://huagongshe.com/ko/reaction/4727
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 2-[4-(3-Chloro-propoxy)-phenyl]-imidazo[1,2-a]pyridine | HCID 14097094 | — |
| 용매 | Dibutylamine | HCID 8148 | — |
| 생성물 | Dibutyl-[3-(4-imidazo[1,2-a]pyridin-2-yl-phenoxy)-propyl]-amine | HCID 10177769 | 192% |
반응 단계
A suspension of 2-(4-chloropropoxyphenyl)imidazo[1,2-a]-pyridine (5.2 g, 14 mmol) in dibutylamine (30 ml) was stirred at reflux for 5 hours. The excess dibutylamine was removed by distillation and the resulting oil was flash chromatographed (silica gel, 9:1 CH2Cl2 : acetone) to give the free base of the title compound (5.1 g, 93% yield) as an oil. The HCl salt was prepared by dropwise addition of concentrated hydrochloric acid to a solution of the free base in methanol, concentrated and recrystallized from methanol acetone to yield 2-(4-dibutylaminopropoxyphenyl)imidazo- [1,2-a]pyridine as a white crystalline solid, mp 179° C. to 183° C. IR(KBr): 3400, 2620, 1650, 1620 cm-1. MS: 380 (MH+). 1H NMR (CD3OD): δ8.80 (d, J=8 Hz, 1H), 8.52 (s, 1H), 7.92-7.49 (m, 5H), 7.18 (d, J=8 Hz, 2H), 4.23 (t, J=4.6 Hz, 2H), 3.50-3.13 (m, 6H), 2.25 (m, 2H), 1.82-1.34 (m, 8H), 1.01 (m, 6H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04727145 |
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| 출처 데이터셋 | uspto-grants-1988_02 |
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| ORD ID | ord-d942c39a6e844fd1a0e45833b16e0d3f |
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| 출처 메모 | uspto-grants-1988_02 |
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