159603-71-1

基本信息
2-叔丁氧羰基氨基-6-氯吡啶
tert-Butyl (6-chloropyridin-2-yl)
2-Amino-6-chloropyridine, 2-Boc protected
ert-Butyl (6-Chloropyridin-2-yl)-carbamate
2-tert-Butoxycarbonylamino-6-chloropyridine
tert-Butyl (6-Chloropyridin-2-yl)-carbamate
tert-Butyl N-(6-chloropyridin-2-yl)carbamate
2-Amino-6-chloropyridine, 2-BOC protected 97%
tert-Butyl (6-Chloropyridin-2-yl)-carbamate ISO 9001:2015 REACH
Carbamic acid, N-(6-chloro-2-pyridinyl)-, 1,1-dimethylethyl ester
物理化學(xué)性質(zhì)
制備方法

45644-21-1

24424-99-5

159603-71-1
在氮氣保護(hù)下,將32.7 g (0.15 mol) 二碳酸二叔丁酯(Boc酸酐)溶解于100 mL四氫呋喃(THF)中,制備成溶液。將此溶液緩慢滴加至含有17.4 g (0.14 mol) 2-氨基-6-氯吡啶和300 mL (0.30 mol) 1 M六甲基二硅氮化鈉的THF溶液(200 mL THF中)的反應(yīng)體系中。反應(yīng)混合物在室溫下攪拌過夜。反應(yīng)完成后,通過旋轉(zhuǎn)蒸發(fā)去除溶劑。將殘余物在乙酸乙酯(EtOAc)和1 N鹽酸水溶液之間分配,充分?jǐn)嚢韬蠓蛛x有機(jī)相。水相再用EtOAc萃取一次。合并所有有機(jī)相,用300 mL飽和碳酸氫鈉溶液洗滌,隨后用無水硫酸鈉干燥,過濾后濃縮。粗產(chǎn)物通過從乙醇(EtOH)中重結(jié)晶純化,得到的固體通過抽濾收集并干燥。最終產(chǎn)物為2-Boc-氨基-6-氯吡啶,產(chǎn)量29.2 g,產(chǎn)率95%。產(chǎn)物通過ESI-MS表征:m/z = 228 (M+),HPLC保留時間(Rt)為1.70 min(方法C)。
參考文獻(xiàn):
[1] Patent: US2011/21500, 2011, A1. Location in patent: Page/Page column 45
[2] Patent: US2011/172218, 2011, A1. Location in patent: Page/Page column 29
[3] Patent: US2012/149698, 2012, A1. Location in patent: Page/Page column 26
[4] Journal of Organic Chemistry, 2005, vol. 70, # 5, p. 1771 - 1779
[5] Patent: US2009/258877, 2009, A1. Location in patent: Page/Page column 16-17