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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2212332생성일: 2026년 10월 26일

Triethylamine → 4-[2-Amino-4-(4-methoxyphenyl)-1,3-thiazol-5-yl]-2-pyridylamine

https://huagongshe.com/reaction/2212332

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물BromineHCID 24408—
반응물ThioureaHCID 2723790—
반응물1-(4-Methoxyphenyl)-2-(2-tert-butoxycarbonylamino-4-pyridyl)ethanoneHCID 11617092—
용매Acetic AcidHCID 176—
생성물4-[2-Amino-4-(4-methoxyphenyl)-1,3-thiazol-5-yl]-2-pyridylamineHCID 996603870%

반응 단계

Bromine (0.68 mL, 13 mmol) was added to a solution of 1-(4-methoxyphenyl)-2-(2-tert-butoxycarbonylamino-4-pyridyl)ethanone (4.5 g, 13 mmol) in acetic acid (100 mL) and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was concentrated. The residue was dissolved in acetonitrile (40 mL) and to the solution was added thiourea (1.1 g, 14 mmol) and triethylamine (1.9 mL, 14 mmol) were added and the mixture was stirred at 80° C. for 2 hours. The reaction mixture was cooled to room temperature and concentrated. A saturated aqueous sodium hydrogencarbonate (200 mL) was added to the residue and the resulting solid was collected by filtration and washed with water. 2N hydrochloric acid (35 mL) was added to the solids and the mixture was stirred at 100° C. for 45 minutes. The reaction mixture was cooled to room temperature and, thereafter, 8N aqueous sodium hydroxide (10 mL) and a saturated aqueous solution of sodium hydrogencarbonate (100 mL) were added. The resulting crude crystals were collected by filtration, and were washed with water. The crude crystals were recrystallized from ethanol to obtain 2.7 g of the title compound (9.1 mmol, yield 69%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07101899B1
출처 데이터셋uspto-grants-2006_09
ORD IDord-316f869261bd4b3b937008a74a7e8211
출처 메모uspto-grants-2006_09