Réaction #4861

ord-1397e52558304bc794ebf0497ed5c6b3

Équation de réaction

Cc1cc(O)cc(C)c1C[C@H](N)C(=O)N[C@H](C)C(=O)O.Cl
title compound
Cc1cc(O)cc(C)c1C[C@H](N)C(=O)N[C@H](C)C(=O)O.Cl
2,6-dimethyltyrosyl-D-alanine, hydrochloride
→
Cc1cc(O)ccc1C[C@H](N)C(=O)N[C@H](C)C(=O)NCCCc1ccccc1.Cl
title compound
Cc1cc(O)ccc1C[C@H](N)C(=O)N[C@H](C)C(=O)NCCCc1ccccc1.Cl
2-methyltyrosyl-N-(3-phenylpropyl)-D-alaninamide, hydrochloride

Réactifs

Cc1cc(O)cc(C)c1C[C@H](N)C(=O)N[C@H](C)C(=O)O.Cl
title compound
Cc1cc(O)cc(C)c1C[C@H](N)C(=O)N[C@H](C)C(=O)O.Cl
2,6-dimethyltyrosyl-D-alanine, hydrochloride

Réactifs

Aucun

Solvants

CO
MeOH

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Mode opératoire

The title compound was prepared by the method of Example 4 from diastereomer F of the title compound of Example 11, Route B. [α]D -23.8 (MeOH)

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US04727189uspto-grants-1988_02