N-(2-amino-5-methylbenzyl)-8-amino-2-methyl-5,11-methano-5,6,11,12-tetrahydrodibenzo[b,f][1,5]diazocine

Base Information

Chemical Name:N-(2-amino-5-methylbenzyl)-8-amino-2-methyl-5,11-methano-5,6,11,12-tetrahydrodibenzo[b,f][1,5]diazocine
CAS No.:334874-39-4
Molecular Formula:C₂₄H₂₆N₄
Molecular Weight:370.497
Hs Code.:

Synonyms:N-(2-amino-5-methylbenzyl)-8-amino-2-methyl-5,11-methano-5,6,11,12-tetrahydrodibenzo[b,f][1,5]diazocine

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Chemical Property of N-(2-amino-5-methylbenzyl)-8-amino-2-methyl-5,11-methano-5,6,11,12-tetrahydrodibenzo[b,f][1,5]diazocine

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Technology Process of N-(2-amino-5-methylbenzyl)-8-amino-2-methyl-5,11-methano-5,6,11,12-tetrahydrodibenzo[b,f][1,5]diazocine

There total 5 articles about N-(2-amino-5-methylbenzyl)-8-amino-2-methyl-5,11-methano-5,6,11,12-tetrahydrodibenzo[b,f][1,5]diazocine 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%

: 334874-40-7
N-(2-amino-5-methylbenzoyl)-8-amino-2-methyl-5,11-methano-5,6,11,12-tetrahydrodibenzo[b,f][1,5]diazocine

: 334874-35-0
8-amino-2-methyl-5,11-methano-5,6,11,12-tetrahydrodibenzo[b,f][1,5]diazocine

: 334874-39-4
N-(2-amino-5-methylbenzyl)-8-amino-2-methyl-5,11-methano-5,6,11,12-tetrahydrodibenzo[b,f][1,5]diazocine

Guidance literature:: With borane-THF; In tetrahydrofuran; for 1h; Heating;
DOI:10.1021/jo0010882

Reference yield:

: 3113-72-2
5-methyl-2-nitrobenzoic acid

: 334874-39-4
N-(2-amino-5-methylbenzyl)-8-amino-2-methyl-5,11-methano-5,6,11,12-tetrahydrodibenzo[b,f][1,5]diazocine

Guidance literature:: Multi-step reaction with 3 steps

1: 66 percent / dicyclohexylcarbodiimide / dimethylformamide / 5 h / 20 °C

2: 98 percent / H₂ / Pd/C / ethanol; CHCl₃ / 3 h / 20 °C / 1520.1 Torr

3: 56 percent / BH₃-THF / tetrahydrofuran / 1 h / Heating

With borane-THF; hydrogen; dicyclohexyl-carbodiimide; palladium on activated charcoal; In tetrahydrofuran; ethanol; chloroform; N,N-dimethyl-formamide;
DOI:10.1021/jo0010882

Reference yield:

: 334874-35-0
8-amino-2-methyl-5,11-methano-5,6,11,12-tetrahydrodibenzo[b,f][1,5]diazocine

: 334874-39-4
N-(2-amino-5-methylbenzyl)-8-amino-2-methyl-5,11-methano-5,6,11,12-tetrahydrodibenzo[b,f][1,5]diazocine

Guidance literature:: Multi-step reaction with 3 steps

1: 66 percent / dicyclohexylcarbodiimide / dimethylformamide / 5 h / 20 °C

2: 98 percent / H₂ / Pd/C / ethanol; CHCl₃ / 3 h / 20 °C / 1520.1 Torr

3: 56 percent / BH₃-THF / tetrahydrofuran / 1 h / Heating

With borane-THF; hydrogen; dicyclohexyl-carbodiimide; palladium on activated charcoal; In tetrahydrofuran; ethanol; chloroform; N,N-dimethyl-formamide;
DOI:10.1021/jo0010882