t-butyl (4-tert-butoxycarbonylmethyl-7-{2-(tert-butoxycarbonylmethyl-amino)-3-[4-(7-nitro-benzo[1,2,5]oxadiazol-4-ylamino)-phenyl]-propyl}-[1,4,7]triazonan-1-yl)-acetate

Base Information

Chemical Name:t-butyl (4-tert-butoxycarbonylmethyl-7-{2-(tert-butoxycarbonylmethyl-amino)-3-[4-(7-nitro-benzo[1,2,5]oxadiazol-4-ylamino)-phenyl]-propyl}-[1,4,7]triazonan-1-yl)-acetate
CAS No.:1016237-85-6
Molecular Formula:C₃₉H₅₈N₈O₉
Molecular Weight:782.938
Hs Code.:

t-butyl (4-tert-butoxycarbonylmethyl-7-{2-(tert-butoxycarbonylmethyl-amino)-3-[4-(7-nitro-benzo[1,2,5]oxadiazol-4-ylamino)-phenyl]-propyl}-[1,4,7]triazonan-1-yl)-acetate

Synonyms:t-butyl (4-tert-butoxycarbonylmethyl-7-{2-(tert-butoxycarbonylmethyl-amino)-3-[4-(7-nitro-benzo[1,2,5]oxadiazol-4-ylamino)-phenyl]-propyl}-[1,4,7]triazonan-1-yl)-acetate

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Chemical Property of t-butyl (4-tert-butoxycarbonylmethyl-7-{2-(tert-butoxycarbonylmethyl-amino)-3-[4-(7-nitro-benzo[1,2,5]oxadiazol-4-ylamino)-phenyl]-propyl}-[1,4,7]triazonan-1-yl)-acetate

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Technology Process of t-butyl (4-tert-butoxycarbonylmethyl-7-{2-(tert-butoxycarbonylmethyl-amino)-3-[4-(7-nitro-benzo[1,2,5]oxadiazol-4-ylamino)-phenyl]-propyl}-[1,4,7]triazonan-1-yl)-acetate

There total 5 articles about t-butyl (4-tert-butoxycarbonylmethyl-7-{2-(tert-butoxycarbonylmethyl-amino)-3-[4-(7-nitro-benzo[1,2,5]oxadiazol-4-ylamino)-phenyl]-propyl}-[1,4,7]triazonan-1-yl)-acetate 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: 26.0%

: 1016237-83-4
tert-butyl {4-[3-(4-amino-phenyl)-2-(tert-butoxycarbonylmethyl-amino)-propyl]-7-tert-butoxycarbonylmethyl-[1,4,7]triazonan-1-yl}-acetate

: 10199-89-0
NBD chloride

: 1016237-85-6
t-butyl (4-tert-butoxycarbonylmethyl-7-{2-(tert-butoxycarbonylmethyl-amino)-3-[4-(7-nitro-benzo[1,2,5]oxadiazol-4-ylamino)-phenyl]-propyl}-[1,4,7]triazonan-1-yl)-acetate

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 24h;
DOI:10.1021/jm701307j

Reference yield:

: tert-butyl {4-tert-butoxycarbonylmethyl-7-[2-(tert-butoxycarbonylmethyl-amino)-3-(4-nitro-phenyl)-propyl]-[1,4,7]-triazonan-1-yl}-acetate

: 1016237-85-6
t-butyl (4-tert-butoxycarbonylmethyl-7-{2-(tert-butoxycarbonylmethyl-amino)-3-[4-(7-nitro-benzo[1,2,5]oxadiazol-4-ylamino)-phenyl]-propyl}-[1,4,7]triazonan-1-yl)-acetate

Guidance literature:: Multi-step reaction with 2 steps

1: palladium 10% on activated carbon; hydrogen / methanol / 14 h / 20 °C / 1034.32 Torr

2: dichloromethane / 4 h / Darkness

With palladium 10% on activated carbon; hydrogen; In methanol; dichloromethane;

Reference yield:

: 1005484-24-1
1,4-di-tert-butyl 7-(2-{[(tert-butoxy)carbonyl]amino}-3-(4-nitrophenyl)propyl)-1,4,7-triazonane-1,4-dicarboxylate

: 1016237-85-6
t-butyl (4-tert-butoxycarbonylmethyl-7-{2-(tert-butoxycarbonylmethyl-amino)-3-[4-(7-nitro-benzo[1,2,5]oxadiazol-4-ylamino)-phenyl]-propyl}-[1,4,7]triazonan-1-yl)-acetate

Guidance literature:: Multi-step reaction with 4 steps

1: trifluoroacetic acid / chloroform / 18 h / 20 °C

2: potassium iodide; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 23.3 h / 0 - 50 °C

3: palladium 10% on activated carbon; hydrogen / methanol / 14 h / 20 °C / 1034.32 Torr

4: dichloromethane / 4 h / Darkness

With palladium 10% on activated carbon; hydrogen; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; potassium iodide; In methanol; dichloromethane; chloroform; N,N-dimethyl-formamide;