Intermediate of API

946511-97-3

  • Product Name:(S)-2-Ethylbutyl 2-aminopropanoate hydrochloride
  • Molecular Formula:
  • Specifications:99%
  • Molecular Weight:209.716
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Product Details;

CasNo: 946511-97-3

Pharmaceutical Intermediates 99% Purity (S)-2-Ethylbutyl 2-aminopropanoate hydrochloride 946511-97-3 Best Price

  • Molecular Formula:C9H19NO2*ClH
  • Molecular Weight:209.716
  • Melting Point:77 - 79°C 

2-ethylbutyl (S)-2-aminopropanoate hydrochloride(Cas 946511-97-3) Usage

Uses

L-Alanine 2-Ethylbutyl Ester Hydrochloride is used in the synthesis of phosphoramidate prodrug of a pyrrolo[2,1-f][triazin-4-amino] adenine C-nucleoside (GS-5734) for the treatment of ebola and emerging viruses.

946511-97-3 Relevant articles

Nucleoside analogue and deuterated substance thereof as well as preparation method and application thereof

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Paragraph 0073-0077, (2021/04/17)

The invention provides a nucleoside anal...

Catalytic Asymmetric Synthesis of the anti-COVID-19 Drug Remdesivir

Chen, Jianzhong,Huo, Xiaohong,Li, Panpan,Wang, Mo,Wu, Zhengxing,Yuan, Qianjia,Zhang, Lu,Zhang, Wanbin,Zhang, Zhenfeng,Zou, Yashi

supporting information, p. 20814 - 20819 (2020/10/15)

The catalytic asymmetric synthesis of th...

THIARABINE- AND THIARABINE PRODRUG-BASED TREATMENTS

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Paragraph 00386, (2020/12/29)

The present disclosure is concerned with...

2,4,7-SUBSTITUTED-7-DEAZA-2'-DEOXY-2'-FLUOROARABINOSYL NUCLEOSIDE AND NUCLEOTIDE PRO-DRUGS AND USES THEREOF

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The present disclosure is concerned with...

946511-97-3 Process route

L-N-Boc-Ala
15761-38-3

L-N-Boc-Ala

2-ethyl-1-butanol
97-95-0

2-ethyl-1-butanol

2-ethylbutyl (S)-2-aminopropanoate hydrochloride
946511-97-3

2-ethylbutyl (S)-2-aminopropanoate hydrochloride

Conditions
Conditions Yield
With chloro-trimethyl-silane; at 20 ℃; for 18h;
85%
With chloro-trimethyl-silane; at 20 ℃; for 18h; Inert atmosphere;
85%
L-alanin
56-41-7,25191-17-7,18875-37-1

L-alanin

2-ethyl-1-butanol
97-95-0

2-ethyl-1-butanol

2-ethylbutyl (S)-2-aminopropanoate hydrochloride
946511-97-3

2-ethylbutyl (S)-2-aminopropanoate hydrochloride

Conditions
Conditions Yield
L-alanin; 2-ethyl-1-butanol; at 0 ℃; for 0.0833333h;
With thionyl chloride; at 60 ℃; for 10h;
80%
2-ethyl-1-butanol; With thionyl chloride; at 0 ℃; for 1h;
L-alanin; at 0 - 90 ℃; for 16h;
74%

946511-97-3 Upstream products

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    1187550-21-5

    C14H27NO4

  • 56-41-7
    56-41-7

    L-alanin

  • 97-95-0
    97-95-0

    2-ethyl-1-butanol

  • 15761-38-3
    15761-38-3

    L-N-Boc-Ala

946511-97-3 Downstream products

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  • 1809249-37-3
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    (2S)-2-ethylbutyl 2-(((S)-(((2R,3S,4R,5R)-5-(4-aminopyrrolo[2,1-f][1,2,4]triazin-7-yl)-5-cyano-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)(phenoxy)phosphoryl)amino)propanoate

  • 1355050-11-1
    1355050-11-1

    (2S)-2-ethylbutyl 2-(((((2R,3S,4R,5R)-5-(4-aminopyrrolo[2,1-f][1,2,4]triazin-7-yl)-5-cyano-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)(phenoxy)phosphoryl)amino)propanoate