1,4-Dimethyl-3-(trityldithio)-3-formyl-6-benzyl-6-(trityltrithio)-2,5-piperazinedione

Base Information

Chemical Name:1,4-Dimethyl-3-(trityldithio)-3-formyl-6-benzyl-6-(trityltrithio)-2,5-piperazinedione
CAS No.:73454-13-4
Molecular Formula:C₅₂H₄₄N₂O₃S₅
Molecular Weight:905.263
Hs Code.:

Synonyms:1,4-Dimethyl-3-(trityldithio)-3-formyl-6-benzyl-6-(trityltrithio)-2,5-piperazinedione

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Chemical Property of 1,4-Dimethyl-3-(trityldithio)-3-formyl-6-benzyl-6-(trityltrithio)-2,5-piperazinedione

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Technology Process of 1,4-Dimethyl-3-(trityldithio)-3-formyl-6-benzyl-6-(trityltrithio)-2,5-piperazinedione

There total 6 articles about 1,4-Dimethyl-3-(trityldithio)-3-formyl-6-benzyl-6-(trityltrithio)-2,5-piperazinedione 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: 100.0%

: 35572-83-9
α,α-diphenylbenzenemethanesulfenyl chloride

: 73454-12-3
1,4-Dimethyl-3-(hydroxymethylene)-6-benzyl-6-(trityltrithio)-2,5-piperazinedione

: 73454-13-4
1,4-Dimethyl-3-(trityldithio)-3-formyl-6-benzyl-6-(trityltrithio)-2,5-piperazinedione

Guidance literature:: With triethylamine; In tetrahydrofuran; at -78 ℃; for 1h;
DOI:10.1021/jo01301a017

Reference yield:

: 5076-82-4
sarcosine anhydride

: 73454-13-4
1,4-Dimethyl-3-(trityldithio)-3-formyl-6-benzyl-6-(trityltrithio)-2,5-piperazinedione

Guidance literature:: Multi-step reaction with 7 steps

1: 95.5 percent / NaOMe / tetrahydrofuran

2: 1) t-BuOK / 1) THF/EtOH, 15min, 0 deg C 2) DMF, 48h, r.t.

3: 1) LDA / 1) THF / -78 deg C / 5 min 2) -78 deg C / 20 min

4: 1) LDA 2) sulfur / 1) THF / -78 deg C / 30 sec 2) THF / -78 deg C / 20 min

5: 69 percent / NEt₃ / tetrahydrofuran / 0.25 h / -78 °C

6: 49 percent / HCl / tetrahydrofuran; CHCl₃; methanol / 6 h

7: 100 percent / Et₃N / tetrahydrofuran / 1 h / -78 °C

With hydrogenchloride; potassium tert-butylate; sodium methylate; sulfur; triethylamine; lithium diisopropyl amide; In tetrahydrofuran; methanol; chloroform;
DOI:10.1021/jo01301a017

Reference yield:

: 73454-05-4
1,4-Dimethyl-3-<<(tert-butyldiphenylsilyl)oxy>methylene>-2,5-piperazinedione

: 73454-13-4
1,4-Dimethyl-3-(trityldithio)-3-formyl-6-benzyl-6-(trityltrithio)-2,5-piperazinedione

Guidance literature:: Multi-step reaction with 5 steps

1: 1) LDA / 1) THF / -78 deg C / 5 min 2) -78 deg C / 20 min

2: 1) LDA 2) sulfur / 1) THF / -78 deg C / 30 sec 2) THF / -78 deg C / 20 min

3: 69 percent / NEt₃ / tetrahydrofuran / 0.25 h / -78 °C

4: 49 percent / HCl / tetrahydrofuran; CHCl₃; methanol / 6 h

5: 100 percent / Et₃N / tetrahydrofuran / 1 h / -78 °C

With hydrogenchloride; sulfur; triethylamine; lithium diisopropyl amide; In tetrahydrofuran; methanol; chloroform;
DOI:10.1021/jo01301a017