(6S,3Z)-4-(4-methoxybenzyl)-1,6-dimethyl-3-(2,4,5-trimethoxy-3-methylbenzylidene)piperazine-2,5-dione

Base Information

Chemical Name:(6S,3Z)-4-(4-methoxybenzyl)-1,6-dimethyl-3-(2,4,5-trimethoxy-3-methylbenzylidene)piperazine-2,5-dione
CAS No.:193686-36-1
Molecular Formula:C₂₅H₃₀N₂O₆
Molecular Weight:454.523
Hs Code.:

Synonyms:(6S,3Z)-4-(4-methoxybenzyl)-1,6-dimethyl-3-(2,4,5-trimethoxy-3-methylbenzylidene)piperazine-2,5-dione

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Chemical Property of (6S,3Z)-4-(4-methoxybenzyl)-1,6-dimethyl-3-(2,4,5-trimethoxy-3-methylbenzylidene)piperazine-2,5-dione

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Technology Process of (6S,3Z)-4-(4-methoxybenzyl)-1,6-dimethyl-3-(2,4,5-trimethoxy-3-methylbenzylidene)piperazine-2,5-dione

There total 6 articles about (6S,3Z)-4-(4-methoxybenzyl)-1,6-dimethyl-3-(2,4,5-trimethoxy-3-methylbenzylidene)piperazine-2,5-dione 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: 86.0%

: 193686-18-9
(6S,3Z)-4-(4-methoxybenzyl)-6-methyl-3-(2,4,5-trimethoxy-3-methylbenzylidene)piperazine-2,5-dione

: 74-88-4
methyl iodide

: 193686-36-1
(6S,3Z)-4-(4-methoxybenzyl)-1,6-dimethyl-3-(2,4,5-trimethoxy-3-methylbenzylidene)piperazine-2,5-dione

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 0 - 25 ℃; for 18h;
DOI:10.3987/COM-18-S(T)88

Reference yield:

: 74124-56-4
(3S)-1,4-diacetyl-3-methylpiperazine-2,5-dione

: 193686-36-1
(6S,3Z)-4-(4-methoxybenzyl)-1,6-dimethyl-3-(2,4,5-trimethoxy-3-methylbenzylidene)piperazine-2,5-dione

Guidance literature:: Multi-step reaction with 4 steps

1: 64.7 percent / potassium tert-butoxide / 2-methyl-propan-2-ol; dimethylformamide / 0.17 h / 0 °C

2: 1.) NaH / 1.) DMF, 30 min, 2.) DMF, RT, 3 h

3: 94.3 percent / hydrazine monohydrate / dimethylformamide / 1 h / Ambient temperature

4: 1.) NaH / 1.) DMF, 0 deg C, 30 min, 2.) DMF, reflux, 3 h

With potassium tert-butylate; sodium hydride; hydrazine hydrate; In N,N-dimethyl-formamide; tert-butyl alcohol;
DOI:10.1248/cpb.45.1120

Reference yield:

: 193686-17-8
(6S,3Z)-1-acetyl-4-(4-methoxybenzyl)-6-methyl-3-(2,4,5-trimethoxy-3-methylbenzylidene)piperazine-2,5-dione

: 193686-36-1
(6S,3Z)-4-(4-methoxybenzyl)-1,6-dimethyl-3-(2,4,5-trimethoxy-3-methylbenzylidene)piperazine-2,5-dione

Guidance literature:: Multi-step reaction with 2 steps

1: 94.3 percent / hydrazine monohydrate / dimethylformamide / 1 h / Ambient temperature

2: 1.) NaH / 1.) DMF, 0 deg C, 30 min, 2.) DMF, reflux, 3 h

With sodium hydride; hydrazine hydrate; In N,N-dimethyl-formamide;
DOI:10.1248/cpb.45.1120