196811-66-2

基本信息
4-(叔丁氧羰基)哌嗪-1-硫代甲酰胺
4-BOC-哌嗪-1-硫酰胺(CAS號(hào):196811-66-2)
1-Boc-4-CarbaMothioylpiperazine
4-(tert-Butoxycarbonyl)piperazine-1-
tert-butyl 4-carbamothioylpiperazine-1-carboxylate
4-(tert-Butoxycarbonyl)piperazine-1-thiocarboxamide
4-THIOCARBAMOYL-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
4-THIOCARBAMOYL-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTE...
1-Piperazinecarboxylic acid, 4-(aMinothioxoMethyl)-, 1,1-diMethylethyl ester
物理化學(xué)性質(zhì)
安全數(shù)據(jù)
制備方法

6160-65-2

57260-71-6

196811-66-2
在室溫下,向N-Boc-哌嗪(5.0 g,26.88 mmol)的無(wú)水THF(50 mL)溶液中加入N,N'-硫羰基二咪唑(5.48 g,29.56 mmol),攪拌反應(yīng)2小時(shí)。隨后,將反應(yīng)混合物加熱至50℃,持續(xù)1小時(shí)。反應(yīng)完成后,將混合物冷卻至0℃,并緩慢加入甲醇氨溶液(50 mL,7 N)。將所得混合物在60℃下攪拌20小時(shí)。反應(yīng)結(jié)束后,用水稀釋反應(yīng)混合物,并用EtOAc進(jìn)行萃取。合并有機(jī)層,用無(wú)水Na2SO4干燥,隨后在真空下濃縮。通過(guò)快速色譜法對(duì)粗產(chǎn)物進(jìn)行純化,得到目標(biāo)化合物4-Boc-哌嗪-1-硫酰胺。產(chǎn)量:4.0 g(92%收率),為白色固體。1H NMR(400 MHz,DMSO-d6)δ:9.2(m,2H),3.16-3.14(m,2H),2.49-2.48(m,6H),1.30(s,9H)。LCMS(方法A):246.2(M + H),保留時(shí)間2.93分鐘,純度95.3%(最大)。
參考文獻(xiàn):
[1] Patent: WO2016/30443, 2016, A1. Location in patent: Page/Page column 106
[2] Patent: WO2017/144637, 2017, A1. Location in patent: Page/Page column 39
[3] Patent: US2010/197703, 2010, A1. Location in patent: Page/Page column 77
[4] Patent: WO2015/48662, 2015, A2. Location in patent: Page/Page column 105
[5] Bioorganic and Medicinal Chemistry, 2008, vol. 16, # 4, p. 1613 - 1631