Reaktion #363679

ord-9910a369e89f4a6a8a28be5f89ac1ca4

Reaktionsgleichung

N[C@H](CO)Cc1ccc(O)cc1
(1S)-1-(4-Hydroxyphenylmethyl)-2-hydroxyethylamine
C1COCN1
oxazolidine
NCCO
2-hydroxyethylamine
CC(C)C1N[C@@H](Cc2ccc(O)cc2)CO1
(4S)-2-isopropyl-4-(4-hydroxyphenylmethyl)-1,3-oxazolidine
CC(C)CN[C@H](CO)Cc1ccc(O)cc1
N-((1S)-1-(4-hydroxyphenylmethyl)-2-hydroxyethyl)-N-isobutylamine
COC(=O)[C@@H](N)Cc1ccc(O)cc1
(L)-tyrosine methyl ester
NCCO
2-hydroxyethylamine
O=S(Cl)Cl
SOCl2
CC(C)C[NH2+][C@H](CCl)Cc1ccc(O)cc1.[Cl-]
N-((1S)-1-(4-hydroxyphenylmethyl)-2-chloroethyl)-N-isobutylammonium chloride

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

(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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06353006B1uspto-grants-2002_03