89673-36-9

基本信息
苯并[B]噻吩-2-基氨基甲酸叔丁酯
tert-Butyl N-(1-benzothiophen-2-yl)carbamate
Benzothiophene-2-carbamic acid tert-butyl ester
Benzo[b]thien-2-yl-carbamic acid tert-butyl ester
物理化學(xué)性質(zhì)
制備方法

6314-28-9

75-65-0

89673-36-9
以苯并[b]噻吩-2-羧酸(1-A,14.4g,80.6mmol)為起始原料,與N,N-二異丙基乙胺(15.5mL,88.6mmol)及二苯基磷酰基疊氮化物(20.8mL,96.7mmol)在叔丁醇(150mL)中混合。將反應(yīng)混合物加熱回流8小時。反應(yīng)完成后,通過真空蒸發(fā)去除溶劑。所得殘余物通過硅膠快速柱色譜法進行純化,以二氯甲烷為洗脫劑,得到目標(biāo)產(chǎn)物苯并[b]噻吩-2-基-氨基甲酸叔丁酯(1-B),為無色固體(18.9g,產(chǎn)率94%)。產(chǎn)物結(jié)構(gòu)經(jīng)1H-NMR(DMSO-d6)和質(zhì)譜(MS)確認:1H-NMR(DMSO-d6)δ 1.50(s, 9H), 6.78(s, 1H), 7.16(d, J=7.5Hz, 1H), 7.27(d, J=7.5Hz, 1H), 7.58(d, J=7.5Hz, 1H), 7.77(d, J=7.5Hz, 1H), 10.70(br s, 1H); MS: m/z 250.2(MH+)。
參考文獻:
[1] Patent: WO2009/12430, 2009, A1. Location in patent: Page/Page column 180-181
[2] Patent: US2010/160289, 2010, A1. Location in patent: Page/Page column 24-25
[3] Patent: US2012/190674, 2012, A1. Location in patent: Page/Page column 73
[4] Patent: US2007/105864, 2007, A1. Location in patent: Page/Page column 193
[5] Patent: US2007/117804, 2007, A1. Location in patent: Page/Page column 125