反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 42.5 °C
PROCEDURE
实验过程
Ortho-chloro-D-tartranilic acid (i.e., (2S,3S)-4-((2-chlorophenyl)amino)-2,3-dihydroxy-4-oxobutanoic acid) (177.5 g, 683.6 mmol) was suspended in water (367 mL) and isopropanol (1.43 L). The mixture was warmed to 40-45° C. over a period of 10 minutes. A solution of 1-(6-bromo-1-methyl-1H-pyrrolo[3,2-b]pyridin-5-yl)ethan-1-amine (170 g, 669 mmol) in IPA was added slowly over a period of 10 minutes while maintaining the temperature of the reaction mixture at 35-45° C. The transfer vessel was rinsed with IPA (100 mL). The IPA rinse was added to the reaction mixture, which was then warmed to 80-85° C. and stirred at this temperature for 15 minutes. The mixture was cooled to 70-75° C. over a period of 30 minutes and a seed of ortho-chloro-D-tartranilic acid salt of (S)-1-(6-bromo-1-methyl-1H-pyrrolo[3,2-b]pyridin-5-yl)ethan-1-amine (350 mg) was added. The reaction mixture was maintained at 70-75° C. for an additional 20 minutes before cooling the mixture to 60-65° C. over a period of 45 minutes. The reaction mixture was maintained at 60-65° C. with stirring for 2 hours before slowly cooling the mixture to 20° C. over a period of 9 hours. The mixture was stirred for 8 hours at 20° C. and then filtered. The solid product was washed with IPA/water (9:1 v/v, 2×510 mL) and then re-suspended in IPA/water (9:1 v/v, 1.19 L). The mixture was warmed to 40-45° C. and maintained at this temperature for 2 hours. The suspension was slowly cooled to 20° C. over a 1 hour period and maintained at 20° C. for 1.5 hours. The reaction mixture was filtered, washed with IPA/water (9:1 v/v, 595 mL), and dried under vacuum at 40° C. to give ortho-chloro-D-tartranilic acid salt of the title compound as a white solid (115.3 g, 99.1% de, 99.6% purity by HPLC).
WORKUP
后处理
- temperaturewhile maintaining the temperature of the reaction mixture at 35-45° C
- washThe transfer vessel was rinsed with IPA (100 mL)
- washThe IPA rinse
- additionwas added to the reaction mixture, which
- temperaturewas then warmed to 80-85° C.
- temperatureThe mixture was cooled to 70-75° C. over a period of 30 minutes
- additiona seed of ortho-chloro-D-tartranilic acid salt of (S)-1-(6-bromo-1-methyl-1H-pyrrolo[3,2-b]pyridin-5-yl)ethan-1-amine (350 mg) was added
- temperatureThe reaction mixture was maintained at 70-75° C. for an additional 20 minutes
- temperaturebefore cooling the mixture to 60-65° C. over a period of 45 minutes
- temperatureThe reaction mixture was maintained at 60-65° C.
- stirringwith stirring for 2 hours
- temperaturebefore slowly cooling the mixture to 20° C. over a period of 9 hours
- stirringThe mixture was stirred for 8 hours at 20° C.
- filtrationfiltered
- washThe solid product was washed with IPA/water (9:1 v/v, 2×510 mL)
- temperatureThe mixture was warmed to 40-45° C.
- temperaturemaintained at this temperature for 2 hours
- temperatureThe suspension was slowly cooled to 20° C. over a 1 hour period
- temperaturemaintained at 20° C. for 1.5 hours
- filtrationThe reaction mixture was filtered
- washwashed with IPA/water (9:1 v/v, 595 mL)
- customdried under vacuum at 40° C.