Triethylamine → HCID 9966038, 화합물

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%).

1. concentrationThe reaction mixture was concentrated
2. dissolutionThe residue was dissolved in acetonitrile (40 mL) and to the solution
3. additionwere added
4. stirringthe mixture was stirred at 80° C. for 2 hours
5. temperatureThe reaction mixture was cooled to room temperature
6. concentrationconcentrated
7. additionA saturated aqueous sodium hydrogencarbonate (200 mL) was added to the residue
8. filtrationthe resulting solid was collected by filtration
9. washwashed with water
10. addition2N hydrochloric acid (35 mL) was added to the solids
11. stirringthe mixture was stirred at 100° C. for 45 minutes
12. temperatureThe reaction mixture was cooled to room temperature
13. addition8N aqueous sodium hydroxide (10 mL) and a saturated aqueous solution of sodium hydrogencarbonate (100 mL) were added
14. filtrationThe resulting crude crystals were collected by filtration
15. washwere washed with water
16. customThe crude crystals were recrystallized from ethanol

ORD 기록

ord-81cc395e52c949fe8c42a9901ab183a8

출처 데이터셋

uspto-grants-2007_10

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US07276527B2