6-Cyclopropylmethoxy-5-methyl-pyridine-2-carboxylic acid → 6-Cyclopropylmethoxy-5-methyl-pyridine-2-carboxylic acid ((S)-2-cyclopropyl-1-thiazol-2-yl-ethyl)-amide
Reaktionsgleichung
C1(COC2N=C(C(O)=O)C=CC=2C)CC1.[CH:16]1([CH2:19][C@H:20]([NH:26][C:27]([C:29]2[CH:34]=[CH:33][C:32]([CH:35]3CCOCC3)=[C:31]([O:41][CH2:42][CH:43]3[CH2:45][CH2:44]3)[N:30]=2)=[O:28])[C:21]2[S:22][CH:23]=[CH:24][N:25]=2)[CH2:18][CH2:17]1>>[CH:16]1([CH2:19][C@H:20]([NH:26][C:27]([C:29]2[CH:34]=[CH:33][C:32]([CH3:35])=[C:31]([O:41][CH2:42][CH:43]3[CH2:45][CH2:44]3)[N:30]=2)=[O:28])[C:21]2[S:22][CH:23]=[CH:24][N:25]=2)[CH2:17][CH2:18]1Komponenten
3
Edukt 2
Produkt 1
Versuchsvorschrift
The title compound was synthesized in analogy to Example 1, using 6-cyclopropylmethoxy-5-methyl-pyridine-2-carboxylic acid (Example 36 d) and (S)-2-cyclopropyl-1-thiazol-2-yl-ethylamine (Example 59 b) as starting materials, MS (LC/MS): 358.2 [M+H]+.
Quellen und Nachweise
- ORD-Eintrag
- ord-21a3eb7a3a3b44d08d67e8d3b63c767b
- Quelldatensatz
- uspto-grants-2016_04
- Patentnummer
- US09321727B2
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