150308-80-8

基本信息
FMOC-SEC(MOB)-OH 1 G
Fmoc-L-Sec(pMeOBzl)-OH
FMOC-SEC(MOB)-OH 250 MG
FMoc-(R)-4-Methoxybenzyl selenocysteine
(9H-Fluoren-9-yl)MethOxy]Carbonyl Sec(Mob)-OH
FMOC-SEC(MOB)-OH
FMOC-R-4-METHOXYBENZYL SELENOCYSTEINE
N-9-fluorenylmethoxycarbonyl-Se-4-methoxybenzylselenocysteine
N-9-fluorenylmethoxycarbonyl-Se-4-methoxybenzylselenocysteine USP/EP/BP
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-[[(4-methoxyphenyl)methyl]seleno]-L-alanine
物理化學(xué)性質(zhì)
制備方法
![L-Alanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-3-[[(4-methoxyphenyl)methyl]seleno]-, methyl ester](/CAS/20210305/GIF/1365284-58-7.gif)
1365284-58-7
![N-芴甲氧羰基-3-[[(4-甲氧基苯基)甲基]硒基]-L-丙氨酸](/CAS/GIF/150308-80-8.gif)
150308-80-8
以化合物(CAS: 1365284-58-7)為原料合成N-芴甲氧羰基-3-[[(4-甲氧基苯基)甲基]硒基]-L-丙氨酸的一般步驟如下:將原料14(790 mg,1.5 mmol)與氫氧化三甲基錫(989 mg,5.5 mmol)的混合物溶解于無(wú)水1,2-二氯乙烷(15 mL)中。反應(yīng)混合物在35℃下攪拌過(guò)夜。反應(yīng)完成后,將混合物過(guò)濾,蒸發(fā)濾液以去除溶劑。所得粗產(chǎn)物通過(guò)硅膠柱色譜法進(jìn)行純化,洗脫劑比例為己烷:EtOAc = 2:1至0:1,得到產(chǎn)物15,為無(wú)色油狀物或白色固體(702 mg,產(chǎn)率91%)。產(chǎn)物15的光譜數(shù)據(jù)與文獻(xiàn)報(bào)道一致37,其純度通過(guò)1H NMR和HPLC分析確認(rèn)。1H NMR(CDCl3)數(shù)據(jù)如下:δ 2.98(2H,m,β-H),3.78(3H,s,p-OMe),3.79(2H,s,CH2),4.26(1H,t,JHH 6.8 Hz,F(xiàn)moc-CH),4.45(1H,d,JHH 6.7 Hz,F(xiàn)moc-CH2),4.70(1H,m,α-H),5.54(1H,d,JHH 7.8 Hz,NH),6.83(2H,d,JHH 8.4 Hz,ArH),7.20(2H,d,JHH 8.3 Hz,ArH),7.33(2H,m,ArH),7.42(2H,m,ArH),7.63(2H,t,JHH 6.7 Hz,ArH),7.78(2H,m,ArH)。13C NMR(CDCl3)數(shù)據(jù)如下:δ 25.1, 27.7, 47.1, 53.6, 55.3, 67.3, 114.1, 120.0, 125.1, 127.1, 127.8, 130.0, 141.3, 143.6, 158.7。77Se NMR(CDCl3)數(shù)據(jù)如下:δ 216.7。
參考文獻(xiàn):
[1] Journal of Peptide Science, 2012, vol. 18, # 3, p. 155 - 162
[2] Arkivoc, 2016, vol. 2017, # 2, p. 260 - 271