97538-67-5 (3R,7aS)-3-(三氯甲基)四氢吡咯并[1,2-c]恶唑-1(3H)-酮
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密封储存,储存于阴凉、干燥的库房。远离氧化剂。旋光度[α]/D 29 to 34°, c = 2 in toluene 沸点338.6±42.0 °C at 760 mmHg 溶解度/溶解性0.334 mg/ml ; 0.00136 mol/l 蒸气压/蒸汽压0.0±0.7 mmHg at 25°C 酸度系数(pKa)2.01±0.40(Predicted) 化学性质无色结晶。熔点 108-112℃。沸点 338.6℃/760mmHg。密度 ρ()1.59g/mL。折光率 n/D1.573。比旋光 [α]/D+29to+34º(c=2,Toluene)。 外观性质白色至近乎白色的无味晶体或粉末,常温下为固体。 步骤:L-脯氨酸(10.0g,86.8mmol)和水合氯醛(21.6g,130mmol)悬浮液在氯仿(100cm³)中,用Dean-Stark分水器回流加热6h;冷却后水洗(2×30cm³),合并有机层干燥(MgSO4),真空除溶剂,得浅棕色固体(19.8g);40℃乙醇(80cm³)重结晶得16.1g(77%)白色固体。条件:回流;6h;氯仿溶剂;乙醇重结晶收率:77%产物:白色固体,mp107-109℃,[α]D+34.2(c=2,C6H6),1H-NMR(200MHz,CDCl3):1.67-2.29(4H,m),3.08-3.20(1H,m),3.37-3.49(1H,m),4.09-4.15(1H,m),5.17(s,1H);13C-NMR(50MHz,CDCl3):25.3(CH2),29.9(CH2),57.9(CH2),62.4(CH),100.6(s),103.6(d),175.5(s);m/z(EI+)=244(MH+)参考文献:[1]European Journal of Organic Chemistry,2013,10,1979-1985;[2]Journal of Organic Chemistry,2012,77,18,7981-7987;[3]Organic Letters,2016,18,8,1888-1891;[4]Tetrahedron,2005,61,42,10018-10035;[5]WO2006/127702,2006,A2;[6]Acta Poloniae Pharmaceutica,2018,75,4,921-927;[7]WO2013/83604,2013,A1;[8]WO2017/201283,2017,A1;[9]WO2017/201285,2017,A1;[10]Angewandte Chemie-International Edition,2017,56,30,8756-8760;[11]Angew.Chem.,2017,129,30,8882-8886;[12]Tetrahedron,1985,41,3,603-610;[13]Angewandte Chemie-International Edition,2001,40,18,3361-3364
- 步骤:向化合物I-K(11.55g,100.3mmol)在500mL氯仿中的悬浮液中加入2,2,2-三氯-1-乙氧基乙醇(23.27g,120.3mmol);Dean-Stark分水器和回流冷凝器下加热回流18h;冷却后减压除溶剂,残余物从EtOH重结晶得15.19g(62%)产物。
- 条件:回流;18h;氯仿溶剂;乙醇重结晶
- 收率:62%
- 产物:白色固体,分子式C7H8Cl3NO2,分子量244.50g·mol⁻¹,[α]20D=+34.3°(c=0.970,苯),熔点109.6℃,1H-NMR(400MHz,CDCl3):δ=1.78-1.64(m,1H,H4'),1.96-1.85(m,1H,H4),2.13-2.02(m,1H,H3'),2.26-2.13(m,1H,H3),3.15-3.06(m,1H,H5'),3.39(ddd,J=10.9,7.8,6.0Hz,1H,H5),4.09(dd,J=8.9,4.6Hz,1H,H2),5.14(s,1H,H7);13C-NMR(100MHz,CDCl3):δ=25.32(t,C4),29.91(t,C3),57.87(t,C5),62.38(t,C2),100.62(s,C8),103.60(d,C7),175.43(s,C6);IR(FT-ATR):2958(m),2920(w),2893(w),2866(w),1784(s),1725(m),1449(w),1373(w),1359(w),1322(m),1283(m),1270(m),1243(m),1174(s),1107(s),1083(m),1043(w),1001(s),958(s),913(w),898(m),838(s),813(s),790(s),744(s)
- 参考文献:[1]Organic Syntheses,2009,86,262-273;[2]WO2011/79114,2011,A1