129799-08-2, 1-tert-Butyl 3-methyl piperazine-1,3-dicarboxylate is a piperazines compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated
EXAMPLE 1; 2-tert-Butyl 8-methyl 6-{[(1S,2R)-1-benzyl-2-hydroxy-3-({1-[3-(trifluoromethyl)phenyl]cyclopropyl}amino)propyl]carbamoyl}-3,4-dihydropyrrolo[1,2-a]pyrazine-2,8(1H)-dicarboxylate; The preparation of pentafluorophenyl formate is described in the literature (Lajos Kisfaludy et al., Synthesis 1987, 5, 510).1.1: 1-tert-Butyl 3-methyl 4-formylpiperazine-1,3-dicarboxylate; 10 g of 2-methoxycarbonyl-4-N-tert-butyl piperazine are dissolved in 25 cm3 of dichloromethane under an inert atmosphere at a temperature close to 20 C. The pentafluorophenyl formate solution obtained in the preceding step is added dropwise at a temperature close to 20 C. Stirring is continued for 1 h 30 min after the end of the addition. The reaction mixture is concentrated using a rotary evaporator under reduced pressure (5 kPa). The yellow-orange oil obtained is purified by flash chromatography through a silica cartridge (column: 700 g; particle size: 40-60 mum; flow rate: 80 cm3/min; eluent: 30% cyclohexane/70% ethyl acetate). After concentrating the fractions under reduced pressure (5 kPa), 10.5 g of 1-tert-butyl 3-methyl 4-formylpiperazine-1,3-dicarboxylate are obtained in the form of a pale yellow oil.NMR: for this batch, a 50%-50% resolution of rotamers is observed with:1.38 (s, 4.5H); 1.39 (s, 4.5H); from 2.62 to 2.93 (m, 1.5H); 3.08 (m, 1H); 3.26 (partially masked m, 0.5H); 3.64 (partially masked m, 0.5H); 3.68 (s, 1.5H); 3.69 (s, 1.5H); 3.90 (m, 1H); 4.02 (m, 0.5H); 4.36 (broad d, J=13.5 Hz, 0.5H); 4.42 (broad d, J=13.5 Hz, 0.5H); 4.71 (broad d, J=4.5 Hz, 0.5H); 4.89 (broad d, J=4.5 Hz, 0.5H); 8.09 (s, 0.5H); 8.16 (s, 0.5H).
129799-08-2, As the paragraph descriping shows that 129799-08-2 is playing an increasingly important role.
Reference:
Patent; SANOFI-AVENTIS; US2010/197668; (2010); A1;,
Piperazine – Wikipedia
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