Reaktion #2507898

ord-4aa10a2d16344848a5f47bef1e98ae62

Reaktionsgleichung

COc1cc(N)ccc1N1CC[C@@H](O)C1
(R)-1-(4-Amino-2-methoxyphenyl)pyrrolidin-3-ol
O=C(O)c1cc(-c2ccc(Cl)cc2)c[nH]1
4-(4-chlorophenyl)-1H-pyrrole-2-carboxylic acid
COc1cc(NC(=O)c2cc(-c3ccc(Cl)cc3)c[nH]2)ccc1N1CC[C@@H](O)C1
title compound
COc1cc(NC(=O)c2cc(-c3ccc(Cl)cc3)c[nH]2)ccc1N1CC[C@@H](O)C1
(R)-4-(4-chlorophenyl)-N-(4-(3-hydroxypyrrolidin-1-yl)-3-methoxyphenyl)-1H-pyrrole-2-carboxamide

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

(R)-1-(4-Amino-2-methoxyphenyl)pyrrolidin-3-ol, preparation described in PCT application WO 2005/042541, was converted to the title compound (48 mg) by acylation with 4-(4-chlorophenyl)-1H-pyrrole-2-carboxylic acid (30 mg) following the procedure described in step C of Example 1. MS (ESI) 412 (M+H)+.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07956049B2uspto-grants-2011_06