(S)-Methyl 4-(1-aminoethyl)benzoate hydrochloride → Methyl 4-((1S)-1-{[5-chloro-2-(3-fluorophenoxy)benzoyl]amino}ethyl)benzoate
Reaktionsgleichung
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:11][C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([F:18])[CH:13]=2)=[C:6]([CH:10]=1)[C:7]([OH:9])=O.Cl.[NH2:20][C@H:21]([C:23]1[CH:32]=[CH:31][C:26]([C:27]([O:29][CH3:30])=[O:28])=[CH:25][CH:24]=1)[CH3:22]>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:11][C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([F:18])[CH:13]=2)=[C:6]([CH:10]=1)[C:7]([NH:20][C@H:21]([C:23]1[CH:32]=[CH:31][C:26]([C:27]([O:29][CH3:30])=[O:28])=[CH:25][CH:24]=1)[CH3:22])=[O:9]Komponenten
3
Versuchsvorschrift
The title compound was prepared according to the procedure described in step 3 of Example 1 from 5-chloro-2-(3-fluorophenoxy)benzoic acid (step 2) and methyl 4-[(1S)-1-aminoethyl]benzoate hydrochloride (step 3 of Example 5): 1H-NMR (CDCl3) δ 8.17 (1H, d, J=2.8 Hz), 7.93 (2H, d, J=8.4 Hz), 7.65 (1H, d, J=7.4 Hz), 7.42–7.26 (4H, m), 6.94–6.88 (2H, m), 6.74–6.65 (2H, m), 5.28 (1H, dq, J=7.4, 7.3 Hz), 3.90 (3H, s), 1.48 (3H, d, J=7.3 Hz).
Quellen und Nachweise
- ORD-Eintrag
- ord-356cce21af6746f79c9f8fa4e2934096