tert-butyl (2S,4R)-2-{[(2S)-2-cyano-1-pyrrolidinyl]carbonyl}-4-(4-hydroxy-2,6-dimethylphenyl)-1-pyrrolidinecarboxylate

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Chemical Name:tert-butyl (2S,4R)-2-{[(2S)-2-cyano-1-pyrrolidinyl]carbonyl}-4-(4-hydroxy-2,6-dimethylphenyl)-1-pyrrolidinecarboxylate
CAS No.:934471-38-2
Molecular Formula:C₂₃H₃₁N₃O₄
Molecular Weight:413.517
Hs Code.:

Synonyms:tert-butyl (2S,4R)-2-{[(2S)-2-cyano-1-pyrrolidinyl]carbonyl}-4-(4-hydroxy-2,6-dimethylphenyl)-1-pyrrolidinecarboxylate

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Chemical Property of tert-butyl (2S,4R)-2-{[(2S)-2-cyano-1-pyrrolidinyl]carbonyl}-4-(4-hydroxy-2,6-dimethylphenyl)-1-pyrrolidinecarboxylate

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Technology Process of tert-butyl (2S,4R)-2-{[(2S)-2-cyano-1-pyrrolidinyl]carbonyl}-4-(4-hydroxy-2,6-dimethylphenyl)-1-pyrrolidinecarboxylate

There total 5 articles about tert-butyl (2S,4R)-2-{[(2S)-2-cyano-1-pyrrolidinyl]carbonyl}-4-(4-hydroxy-2,6-dimethylphenyl)-1-pyrrolidinecarboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 56.0%

: 934471-37-1
tert-butyl (2S,4R)-4-(2-benzyloxy-2,6-dimethylphenyl)-2-{[(2S)-2-cyano-1-pyrrolidinyl]carbonyl}-1-pyrrolidinecarboxylate

: 934471-38-2
tert-butyl (2S,4R)-2-{[(2S)-2-cyano-1-pyrrolidinyl]carbonyl}-4-(4-hydroxy-2,6-dimethylphenyl)-1-pyrrolidinecarboxylate

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; at 20 ℃; for 5h; atmospheric pressure;
DOI:10.1016/j.bmc.2007.01.033

Reference yield:

: 1-tert-butyl 2-methyl (2S)-4-(4-benzyloxy-2,6-dimethylphenyl)-2,5-dihydro-1H-pyrrole-1,2-dicarboxylate

: 934471-38-2
tert-butyl (2S,4R)-2-{[(2S)-2-cyano-1-pyrrolidinyl]carbonyl}-4-(4-hydroxy-2,6-dimethylphenyl)-1-pyrrolidinecarboxylate

Guidance literature:: Multi-step reaction with 5 steps

1: 92 percent / hydrogen / Pd/C / methanol / 13 h / 20 °C / atmospheric pressure

2: 79 percent / K₂CO₃ / dimethylformamide / 15 h / 20 °C

3: 100 percent / NaOH / methanol; H₂O / 6 h / 20 °C

4: 93 percent / 1-methanesulfonyloxy-1H-benzotriazole; triethylamine / dimethylformamide / 15 h / 20 °C

5: 56 percent / hydrogen / Pd/C / methanol / 5 h / 20 °C / atmospheric pressure

With sodium hydroxide; hydrogen; potassium carbonate; triethylamine; palladium on activated charcoal; In methanol; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2007.01.033

Reference yield:

: 934471-24-6
(2S,4R)-4-(4-benzyloxy-2,6-dimethylphenyl)-1-(tert-butoxycarbonyl)-2-pyrrolidinecarboxylic acid

: 934471-38-2
tert-butyl (2S,4R)-2-{[(2S)-2-cyano-1-pyrrolidinyl]carbonyl}-4-(4-hydroxy-2,6-dimethylphenyl)-1-pyrrolidinecarboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: 93 percent / 1-methanesulfonyloxy-1H-benzotriazole; triethylamine / dimethylformamide / 15 h / 20 °C

2: 56 percent / hydrogen / Pd/C / methanol / 5 h / 20 °C / atmospheric pressure

With hydrogen; triethylamine; palladium on activated charcoal; In methanol; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2007.01.033