Reaktionsgleichung
[Cl:1][C:2]1[CH:16]=[CH:15][C:5]2[N:6]=[C:7]([NH:9][CH:10]3[CH2:14][CH2:13][NH:12][CH2:11]3)[O:8][C:4]=2[CH:3]=1.Cl.ClC1OC2C=C(Cl)C=CC=2N=1>>[ClH:1].[Cl:1][C:2]1[CH:16]=[CH:15][C:5]2[N:6]=[C:7]([NH:9][C@@H:10]3[CH2:14][CH2:13][NH:12][CH2:11]3)[O:8][C:4]=2[CH:3]=1Komponenten
4
Versuchsvorschrift
In analogy to the procedure described for the synthesis of (6-Chloro-benzooxazol-2-yl)-pyrrolidin-3-yl-amine; hydrochloride (example 1, step 1) the title compound was prepared from 2,6-dichloro-benzoxazole (commercially available) and R-3-amino-pyrrolidine-1-carboxylic acid tert-butyl ester (commercially available) and subsequent cleavage of the tert-butyl oxy carbonyl protecting group under acidic conditions. (MH+) 238.0.
Quellen und Nachweise
- ORD-Eintrag
- ord-4269e0b778fa46ffacdf267cba5921d7
- Quelldatensatz
- uspto-grants-2011_03
- Patentnummer
- US07897627B2
Verknüpfte Notizen
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