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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276499Generated: October 25, 2026

Ethanolamine → N-((1S)-1-(4-chlorophenylmethyl)-2-chloroethyl)-N-isobutylammonium chloride

https://huagongshe.com/reaction/276499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantThionyl ChlorideHCID 24386—
Reactant1,3-OxazolidineHCID 536683—
Reactant(S)-2-Amino-3-(4-chlorophenyl)propan-1-OLHCID 719509—
Reactant(4S)-2-isopropyl-4-(4-chlorophenylmethyl)-1,3-oxazolidineHCID 57189183—
ReactantN-((1S)-1-(4-chlorophenylmethyl)-2-hydroxyethyl)-N-isobutylamineHCID 69993392—
ProductN-((1S)-1-(4-chlorophenylmethyl)-2-chloroethyl)-N-isobutylammonium chlorideHCID 22951241—

Reaction Steps

(1S)-1-(4-Chlorophenylmethyl)-2-hydroxyethylamine was made from (L)-4-chlorophenylalanine methyl ester as described in Method B1b. The 2-hydroxyethylamine was converted to (4S)-2-isopropyl-4-(4-chlorophenylmethyl)-1,3-oxazolidine according to Method B4c, Step 1. The oxazolidine was reduced to N-((1S)-1-(4-chlorophenylmethyl)-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-chlorophenylmethyl)-2-chloroethyl)-N-isobutylammonium chloride. 2-Ethyl-4-cyanophenyl isothiocyanate was reacted with N-((1S)-1-(4-chlorophenylmethyl)-2-chloroethyl)-N isobutylammonium chloride according to Method C1b to give (4S)-2-(2-ethyl-4-cyanophenylimino)-4-(4-chlorophenylmethyl)-3-isobutyl-1,3-thiazolidine HCl salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06353006B1
Source datasetuspto-grants-2002_03
ORD IDord-dc036e81bb9448f2b749aafb9919532d
Source noteuspto-grants-2002_03