(S)-2-Amino-N-[4-(4-{[(2,2-dichloro-acetyl)-(2-ethoxy-ethyl)-amino]-methyl}-phenoxy)-phenyl]-4-methylsulfanyl-butyramide; hydrochloride

Base Information

Chemical Name:(S)-2-Amino-N-[4-(4-{[(2,2-dichloro-acetyl)-(2-ethoxy-ethyl)-amino]-methyl}-phenoxy)-phenyl]-4-methylsulfanyl-butyramide; hydrochloride
CAS No.:70718-52-4
Molecular Formula:C₂₄H₃₁Cl₂N₃O₄S*ClH
Molecular Weight:564.961
Hs Code.:

Synonyms:

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Chemical Property of (S)-2-Amino-N-[4-(4-{[(2,2-dichloro-acetyl)-(2-ethoxy-ethyl)-amino]-methyl}-phenoxy)-phenyl]-4-methylsulfanyl-butyramide; hydrochloride

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Technology Process of (S)-2-Amino-N-[4-(4-{[(2,2-dichloro-acetyl)-(2-ethoxy-ethyl)-amino]-methyl}-phenoxy)-phenyl]-4-methylsulfanyl-butyramide; hydrochloride

There total 4 articles about (S)-2-Amino-N-[4-(4-{[(2,2-dichloro-acetyl)-(2-ethoxy-ethyl)-amino]-methyl}-phenoxy)-phenyl]-4-methylsulfanyl-butyramide; hydrochloride 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:

: 70718-61-5
{(S)-1-[4-(4-{[(2,2-Dichloro-acetyl)-(2-ethoxy-ethyl)-amino]-methyl}-phenoxy)-phenylcarbamoyl]-3-methylsulfanyl-propyl}-carbamic acid tert-butyl ester

: 70718-52-4
(S)-2-Amino-N-[4-(4-{[(2,2-dichloro-acetyl)-(2-ethoxy-ethyl)-amino]-methyl}-phenoxy)-phenyl]-4-methylsulfanyl-butyramide; hydrochloride

Guidance literature:: With hydrogenchloride; In ethanol; ethyl acetate; for 4h; Ambient temperature;

Reference yield:

: 2488-15-5
N-tert-butoxycarbonyl-L-methionine

: 70718-52-4
(S)-2-Amino-N-[4-(4-{[(2,2-dichloro-acetyl)-(2-ethoxy-ethyl)-amino]-methyl}-phenoxy)-phenyl]-4-methylsulfanyl-butyramide; hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: pivaloyl chloride, triethylamine / acetone / 3 h / Ambient temperature

2: 3percent HCl / ethanol; ethyl acetate / 4 h / Ambient temperature

With hydrogenchloride; pivaloyl chloride; triethylamine; In ethanol; ethyl acetate; acetone;

Reference yield:

: 70718-44-4
N-(2-ethoxyethyl)-N-<4-(4-aminophenoxy) benzyl> dichloroacetamide

: 70718-52-4
(S)-2-Amino-N-[4-(4-{[(2,2-dichloro-acetyl)-(2-ethoxy-ethyl)-amino]-methyl}-phenoxy)-phenyl]-4-methylsulfanyl-butyramide; hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: pivaloyl chloride, triethylamine / acetone / 3 h / Ambient temperature

2: 3percent HCl / ethanol; ethyl acetate / 4 h / Ambient temperature

With hydrogenchloride; pivaloyl chloride; triethylamine; In ethanol; ethyl acetate; acetone;