Reaktionsgleichung
Cl.[N:2]1([C:8]([NH2:10])=[O:9])[CH2:7][CH2:6][O:5][CH2:4][CH2:3]1.[NH2:11][CH:12]1[CH2:20][C:19]2[C:14](=[CH:15][CH:16]=[C:17]([C:21]([OH:23])=[O:22])[CH:18]=2)[CH2:13]1.C(N(CC)CC)C.Cl[C:32]1[C:33]2[C:40]([CH3:41])=[CH:39][S:38][C:34]=2[N:35]=[CH:36][N:37]=1>C(O)C>[N:2]1([C:8]([NH2:10])=[O:9])[CH2:7][CH2:6][O:5][CH2:4][CH2:3]1.[CH3:41][C:40]1[C:33]2[C:32]([NH:11][CH:12]3[CH2:20][C:19]4[C:14](=[CH:15][CH:16]=[C:17]([C:21]([OH:23])=[O:22])[CH:18]=4)[CH2:13]3)=[N:37][CH:36]=[N:35][C:34]=2[S:38][CH:39]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Using 2-aminoindan-5-carboxylic acid morpholinamide hydrochloride (750 mg, 2.7 mmol), ethanol (23 ml), triethylamine (1.1 ml, 8.2 mmol), and 4-chloro-5-methylthieno[2,3-d]pyrimidine (500 mg, 2.7 mmol), a similar procedure to b) in Production Example 208 was carried out. The product obtained was purified by silica gel chromatography (methylene chloride:methanol=95:5) to yield a fraction, which was then washed with ether to obtain the title compound (680 mg, 1.7 mmol) having the following physical properties:
Aufarbeitung
- customThe product obtained
- customwas purified by silica gel chromatography (methylene chloride:methanol=95:5)
- customto yield a fraction, which
- washwas then washed with ether
Quellen und Nachweise
- ORD-Eintrag
- ord-809fdd9988a440ba8ee2240257153fb3
- Quelldatensatz
- uspto-grants-2004_03
- Patentnummer
- US06703421B1
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