{(R)-1-[4-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-phenylcarbamoyl]-2-naphthalen-2-yl-ethyl}-carbamic acid tert-butyl ester

Base Information

Chemical Name:{(R)-1-[4-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-phenylcarbamoyl]-2-naphthalen-2-yl-ethyl}-carbamic acid tert-butyl ester
CAS No.:195717-40-9
Molecular Formula:C₃₃H₃₁N₃O₅
Molecular Weight:549.626
Hs Code.:

Synonyms:{(R)-1-[4-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-phenylcarbamoyl]-2-naphthalen-2-yl-ethyl}-carbamic acid tert-butyl ester

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Chemical Property of {(R)-1-[4-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-phenylcarbamoyl]-2-naphthalen-2-yl-ethyl}-carbamic acid tert-butyl ester

Chemical Property:

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Technology Process of {(R)-1-[4-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-phenylcarbamoyl]-2-naphthalen-2-yl-ethyl}-carbamic acid tert-butyl ester

There total 1 articles about {(R)-1-[4-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-phenylcarbamoyl]-2-naphthalen-2-yl-ethyl}-carbamic acid tert-butyl ester 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:

: 4403-71-8
(4-aminomethyl)aniline

: 195717-40-9
{(R)-1-[4-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-phenylcarbamoyl]-2-naphthalen-2-yl-ethyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: tetra(n-butyl)ammonium hydrogensulfate; sodium hydrogencarbonate / dichloromethane

2: benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide / N,N-dimethyl-formamide

With tetra(n-butyl)ammonium hydrogensulfate; sodium hydrogencarbonate; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0960-894X(97)00328-4

Reference yield:

: 195717-40-9
{(R)-1-[4-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-phenylcarbamoyl]-2-naphthalen-2-yl-ethyl}-carbamic acid tert-butyl ester

: (S)-2-Amino-5-guanidino-pentanoic acid 4-[(R)-2-(N',N''-dicyclohexyl-guanidino)-3-naphthalen-2-yl-propionylamino]-benzylamide; hydrochloride

Guidance literature:: Multi-step reaction with 5 steps

1: hydrogenchloride / ethyl acetate

2: triethylamine; dicyclohexyl-carbodiimide / tert-butyl alcohol / 80 °C

3: hydrazine hydrate / methanol

4: benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide

5: hydrogenchloride / ethyl acetate

With hydrogenchloride; benzotriazol-1-ol; hydrazine hydrate; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; In methanol; ethyl acetate; N,N-dimethyl-formamide; tert-butyl alcohol;
DOI:10.1016/S0960-894X(97)00328-4

Reference yield:

: 195717-40-9
{(R)-1-[4-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-phenylcarbamoyl]-2-naphthalen-2-yl-ethyl}-carbamic acid tert-butyl ester

: 195716-40-6
(R)-N-(4-Aminomethyl-phenyl)-2-(N',N''-dicyclohexyl-guanidino)-3-naphthalen-2-yl-propionamide

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogenchloride / ethyl acetate

2: triethylamine; dicyclohexyl-carbodiimide / tert-butyl alcohol / 80 °C

3: hydrazine hydrate / methanol

With hydrogenchloride; hydrazine hydrate; triethylamine; dicyclohexyl-carbodiimide; In methanol; ethyl acetate; tert-butyl alcohol;
DOI:10.1016/S0960-894X(97)00328-4