N-t-butyloxycarbonyl-N-phenylmethyl-1-(1-oxo-4-pentynyl)-1H-indole-3-ethanamine

Base Information

Chemical Name:N-t-butyloxycarbonyl-N-phenylmethyl-1-(1-oxo-4-pentynyl)-1H-indole-3-ethanamine
CAS No.:371246-09-2
Molecular Formula:C₂₇H₃₀N₂O₃
Molecular Weight:430.547
Hs Code.:

Synonyms:N-t-butyloxycarbonyl-N-phenylmethyl-1-(1-oxo-4-pentynyl)-1H-indole-3-ethanamine

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Chemical Property of N-t-butyloxycarbonyl-N-phenylmethyl-1-(1-oxo-4-pentynyl)-1H-indole-3-ethanamine

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Technology Process of N-t-butyloxycarbonyl-N-phenylmethyl-1-(1-oxo-4-pentynyl)-1H-indole-3-ethanamine

There total 4 articles about N-t-butyloxycarbonyl-N-phenylmethyl-1-(1-oxo-4-pentynyl)-1H-indole-3-ethanamine 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: 74.0%

: 55183-44-3
4-pentynoic chloride

: 371246-08-1
N-t-butyloxycarbonyl-N-(phenylmethyl)-1H-indole-3-ethanamine

: 371246-09-2
N-t-butyloxycarbonyl-N-phenylmethyl-1-(1-oxo-4-pentynyl)-1H-indole-3-ethanamine

Guidance literature:: N-t-butyloxycarbonyl-N-(phenylmethyl)-1H-indole-3-ethanamine; With potassium hydroxide; In 1,2-dimethoxyethane; for 0.333333h;

4-pentynoic chloride; In 1,2-dimethoxyethane; at 0 ℃; for 0.0333333h; Further stages.;
DOI:10.1021/ja016333t

Reference yield:

: 61-54-1
tryptamine

: 371246-09-2
N-t-butyloxycarbonyl-N-phenylmethyl-1-(1-oxo-4-pentynyl)-1H-indole-3-ethanamine

Guidance literature:: Multi-step reaction with 3 steps

1.1: methanol / 1 h / 25 °C

1.2: NaBH₄ / methanol / 0.08 h / 25 °C

2.1: 13.2 g / CH₂Cl₂ / 0.5 h / 25 °C

3.1: KOH / 1,2-dimethoxy-ethane / 0.33 h

3.2: 74 percent / 1,2-dimethoxy-ethane / 0.03 h / 0 °C

With potassium hydroxide; In methanol; 1,2-dimethoxyethane; dichloromethane;
DOI:10.1021/ja016333t

Reference yield:

: 15741-79-4
N-benzyl tryptamine

: 371246-09-2
N-t-butyloxycarbonyl-N-phenylmethyl-1-(1-oxo-4-pentynyl)-1H-indole-3-ethanamine

Guidance literature:: Multi-step reaction with 2 steps

1.1: 13.2 g / CH₂Cl₂ / 0.5 h / 25 °C

2.1: KOH / 1,2-dimethoxy-ethane / 0.33 h

2.2: 74 percent / 1,2-dimethoxy-ethane / 0.03 h / 0 °C

With potassium hydroxide; In 1,2-dimethoxyethane; dichloromethane;
DOI:10.1021/ja016333t