24391-41-1

基本信息
4-氯-7H-吡咯并[2,3-D]嘧啶-5-甲腈
4-氯-7H-吡咯并[2,3-D]嘧啶-5-氰基
4-Chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile
7H-Pyrrolo[2,3-d]pyriMidine-5-carbonitrile,4-chloro-
物理化學(xué)性質(zhì)
安全數(shù)據(jù)
制備方法

908287-23-0
![4-氯-7H-吡咯[2,3-D]嘧啶-5-甲腈](/CAS/GIF/24391-41-1.gif)
24391-41-1
向4-氯-7H-吡咯并[2,3-d]嘧啶-5-甲醛肟(865 mg,4.40 mmol,1.0當(dāng)量)在二氯甲烷(20 mL)中的懸浮液中緩慢加入亞硫酰氯(3.1 mL,43.7 mmol,10.0當(dāng)量)。將反應(yīng)混合物在室溫下攪拌過(guò)夜。反應(yīng)完成后,將混合物在減壓下濃縮以除去溶劑。將殘余物懸浮于水(60 mL)中,緩慢加入飽和碳酸氫鈉水溶液調(diào)節(jié)pH至4。通過(guò)抽濾收集析出的固體,依次用水和乙酸乙酯洗滌,得到第一批產(chǎn)物。隨后,用乙酸乙酯(50 mL×3)萃取濾液。合并有機(jī)相,用飽和食鹽水洗滌,無(wú)水硫酸鈉干燥,過(guò)濾。濾液減壓濃縮,所得殘余物與前述固體合并。粗產(chǎn)物在乙酸乙酯/己烷(1:1,v/v)混合溶劑中重結(jié)晶,減壓干燥,得到4-氯-7H-吡咯并[2,3-d]嘧啶-5-甲腈(763 mg,收率97%)。ESI-MS m/z: 178.8 [M + H]+, 176.8 [M - H]+。
參考文獻(xiàn):
[1] Patent: WO2013/12915, 2013, A1. Location in patent: Paragraph 00942
[2] Patent: WO2008/12635, 2008, A2. Location in patent: Page/Page column 83
[3] Patent: US2009/5359, 2009, A1. Location in patent: Page/Page column 25
[4] Patent: WO2011/146882, 2011, A1. Location in patent: Page/Page column 110-111
[5] Patent: US2012/122838, 2012, A1. Location in patent: Page/Page column 81-82