[4-(1-allyl-1H-indol-6-yl)pyrimidin-2-yl]-[3-allyloxymethyl-4-(2-pyrrolidin-1-ylethoxy)phenyl]amine

Base Information

Chemical Name:[4-(1-allyl-1H-indol-6-yl)pyrimidin-2-yl]-[3-allyloxymethyl-4-(2-pyrrolidin-1-ylethoxy)phenyl]amine
CAS No.:1027635-72-8
Molecular Formula:C₃₁H₃₅N₅O₂
Molecular Weight:509.651
Hs Code.:

Synonyms:[4-(1-allyl-1H-indol-6-yl)pyrimidin-2-yl]-[3-allyloxymethyl-4-(2-pyrrolidin-1-ylethoxy)phenyl]amine

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Chemical Property of [4-(1-allyl-1H-indol-6-yl)pyrimidin-2-yl]-[3-allyloxymethyl-4-(2-pyrrolidin-1-ylethoxy)phenyl]amine

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Technology Process of [4-(1-allyl-1H-indol-6-yl)pyrimidin-2-yl]-[3-allyloxymethyl-4-(2-pyrrolidin-1-ylethoxy)phenyl]amine

There total 8 articles about [4-(1-allyl-1H-indol-6-yl)pyrimidin-2-yl]-[3-allyloxymethyl-4-(2-pyrrolidin-1-ylethoxy)phenyl]amine 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: 71.0%

: 937273-33-1
3-allyloxymethyl-4-(2-pyrrolidin-1-yl-ethoxy)phenylamine

: 1027635-70-6
1-allyl-6-(2-chloropyrimidin-4-yl)-1H-indole

: 1027635-72-8
[4-(1-allyl-1H-indol-6-yl)pyrimidin-2-yl]-[3-allyloxymethyl-4-(2-pyrrolidin-1-ylethoxy)phenyl]amine

Guidance literature:: With hydrogenchloride; water; In butan-1-ol; at 80 - 100 ℃; for 12h;
DOI:10.1021/jm201454n

Reference yield:

: 147621-18-9
6-indolylboronic acid

: 1027635-72-8
[4-(1-allyl-1H-indol-6-yl)pyrimidin-2-yl]-[3-allyloxymethyl-4-(2-pyrrolidin-1-ylethoxy)phenyl]amine

Guidance literature:: Multi-step reaction with 3 steps

1.1: tetrakis(triphenylphosphine) palladium⁽⁰⁾; water; sodium hydrogencarbonate / 1,2-dimethoxyethane / 6 h / 85 °C

2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 20 °C

2.2: 20 °C

3.1: hydrogenchloride; water / butan-1-ol / 12 h / 80 - 100 °C

With hydrogenchloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; water; sodium hydride; sodium hydrogencarbonate; In 1,2-dimethoxyethane; N,N-dimethyl-formamide; mineral oil; butan-1-ol; 1.1: Suzuki coupling;
DOI:10.1021/jm201454n

Reference yield:

: 937273-30-8
[2-(2-chloroethoxy)-5-nitrophenyl]methanol

: 1027635-72-8
[4-(1-allyl-1H-indol-6-yl)pyrimidin-2-yl]-[3-allyloxymethyl-4-(2-pyrrolidin-1-ylethoxy)phenyl]amine

Guidance literature:: Multi-step reaction with 4 steps

1: tetra(n-butyl)ammonium hydrogensulfate; potassium hydroxide / 12 h / 20 °C

2: N,N-dimethyl acetamide / 20 h / 90 °C

3: tin(II) chloride dihdyrate / methanol; dichloromethane / 0 - 20 °C

4: hydrogenchloride; water / butan-1-ol / 12 h / 80 - 100 °C

With hydrogenchloride; tin(II) chloride dihdyrate; water; tetra(n-butyl)ammonium hydrogensulfate; potassium hydroxide; In methanol; dichloromethane; N,N-dimethyl acetamide; butan-1-ol;
DOI:10.1021/jm201454n