HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276497Erstellt: 24. Oktober 2026
Ethanolamine → N-((1S)-1-(4-hydroxyphenylmethyl)-2-chloroethyl)-N-isobutylammonium chloride
https://huagongshe.com/de/reaction/276497
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethanolamine | HCID 700 | — |
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Edukt | Tyrosine Methyl Ester | HCID 70652 | — |
| Edukt | Tyrosinol | HCID 151247 | — |
| Edukt | 1,3-Oxazolidine | HCID 536683 | — |
| Edukt | N-((1S)-1-(4-hydroxyphenylmethyl)-2-hydroxyethyl)-N-isobutylamine | HCID 54421810 | — |
| Edukt | (4S)-2-isopropyl-4-(4-hydroxyphenylmethyl)-1,3-oxazolidine | HCID 57008578 | — |
| Produkt | N-((1S)-1-(4-hydroxyphenylmethyl)-2-chloroethyl)-N-isobutylammonium chloride | HCID 69992632 | — |
Reaktionsschritte
(1S)-1-(4-Hydroxyphenylmethyl)-2-hydroxyethylamine was made from (L)-tyrosine methyl ester as described in Method B1b. The 2-hydroxyethylamine was converted to (4S)-2-isopropyl-4-(4-hydroxyphenylmethyl)-1,3-oxazolidine according to Method B4c, Step 1. The oxazolidine was reduced to N-((1S)-1-(4-hydroxyphenylmethyl)-2-hydroxyethyl)-N-isobutylamine according to Method B4c, Step 2. The resulting 2-hydroxyethylamine was treated with SOCl2 according to Method B7c to give N-((1S)-1-(4-hydroxyphenylmethyl)-2-chloroethyl)-N-isobutylammonium chloride. 2-Ethyl-4-cyanophenyl isothiocyanate was reacted with N-((1S)-1-(4-hydroxyphenylmethyl)-2-chloroethyl)-N-isobutylammonium chloride according to Method C1b to give (4S)-2-(2-ethyl-4-cyanophenylimino)-4-(4-hydroxyphenylmethyl)-3-isobutyl-1,3-thiazolidine HCl salt.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06353006B1 |
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| Quelldatensatz | uspto-grants-2002_03 |
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| ORD ID | ord-9910a369e89f4a6a8a28be5f89ac1ca4 |
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| Quellennotiz | uspto-grants-2002_03 |
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