17-cyclopropylmethyl-6,7-didehydro-4,5α-epoxy-5'-bis-tert-butoxycarbonyl-(N'-4-nitrobenzyl)guanidinylethyl-3,14-dihydroxyindolo[2',3':6,7]morphinan

Base Information

Chemical Name:17-cyclopropylmethyl-6,7-didehydro-4,5α-epoxy-5'-bis-tert-butoxycarbonyl-(N'-4-nitrobenzyl)guanidinylethyl-3,14-dihydroxyindolo[2',3':6,7]morphinan
CAS No.:641611-27-0
Molecular Formula:C₄₆H₅₄N₆O₉
Molecular Weight:834.97
Hs Code.:

17-cyclopropylmethyl-6,7-didehydro-4,5α-epoxy-5'-bis-tert-butoxycarbonyl-(N'-4-nitrobenzyl)guanidinylethyl-3,14-dihydroxyindolo[2',3':6,7]morphinan

Synonyms:17-cyclopropylmethyl-6,7-didehydro-4,5α-epoxy-5'-bis-tert-butoxycarbonyl-(N'-4-nitrobenzyl)guanidinylethyl-3,14-dihydroxyindolo[2',3':6,7]morphinan

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Chemical Property of 17-cyclopropylmethyl-6,7-didehydro-4,5α-epoxy-5'-bis-tert-butoxycarbonyl-(N'-4-nitrobenzyl)guanidinylethyl-3,14-dihydroxyindolo[2',3':6,7]morphinan

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Technology Process of 17-cyclopropylmethyl-6,7-didehydro-4,5α-epoxy-5'-bis-tert-butoxycarbonyl-(N'-4-nitrobenzyl)guanidinylethyl-3,14-dihydroxyindolo[2',3':6,7]morphinan

There total 2 articles about 17-cyclopropylmethyl-6,7-didehydro-4,5α-epoxy-5'-bis-tert-butoxycarbonyl-(N'-4-nitrobenzyl)guanidinylethyl-3,14-dihydroxyindolo[2',3':6,7]morphinan 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:

: 107819-90-9
1,3-bis(tert-butoxycarbonyl)-2-methyl-2-thiopseudourea

: 641611-27-0
17-cyclopropylmethyl-6,7-didehydro-4,5α-epoxy-5'-bis-tert-butoxycarbonyl-(N'-4-nitrobenzyl)guanidinylethyl-3,14-dihydroxyindolo[2',3':6,7]morphinan

Guidance literature:: Multi-step reaction with 2 steps

1.1: NaH / dimethylformamide / 1 h / cooling

1.2: 75 percent / dimethylformamide / 12 h / 20 °C

2.1: 44 percent / HgCl₂; Et₃N / dimethylformamide / 12 h / 50 °C

With sodium hydride; triethylamine; mercury dichloride; In N,N-dimethyl-formamide;
DOI:10.1021/jm0309203

Reference yield:

: 100-11-8
1-bromomethyl-4-nitro-benzene

: 641611-27-0
17-cyclopropylmethyl-6,7-didehydro-4,5α-epoxy-5'-bis-tert-butoxycarbonyl-(N'-4-nitrobenzyl)guanidinylethyl-3,14-dihydroxyindolo[2',3':6,7]morphinan

Guidance literature:: Multi-step reaction with 2 steps

1.1: NaH / dimethylformamide / 1 h / cooling

1.2: 75 percent / dimethylformamide / 12 h / 20 °C

2.1: 44 percent / HgCl₂; Et₃N / dimethylformamide / 12 h / 50 °C

With sodium hydride; triethylamine; mercury dichloride; In N,N-dimethyl-formamide;
DOI:10.1021/jm0309203