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HRID 17208Erstellt: 24. Oktober 2026
Aminoacetaldehyde dimethyl acetal → 4-Amino-N-(2,2-dimethoxyethyl)-3-(3-methoxy-4-{[(1-methyl-1H-indol-2-yl)carbonyl]amino}phenyl)thieno[3,2-c]pyridine-7-carboxamide
https://huagongshe.com/de/reaction/17208
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Edukt | Carbonic acid--N,N-diethylethanamine (1/2) | HCID 15264167 | — |
| Edukt | 4-amino-3-(3-methoxy-4-(1-methyl-1H-indole-2-carboxamido)phenyl)thieno[3,2-c]pyridine-7-carboxylic acid | HCID 18450830 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Produkt | 4-Amino-N-(2,2-dimethoxyethyl)-3-(3-methoxy-4-{[(1-methyl-1H-indol-2-yl)carbonyl]amino}phenyl)thieno[3,2-c]pyridine-7-carboxamide | HCID 18450840 | 71% |
Reaktionsschritte
4-amino-3-(3-methoxy-4-{[(1-methyl-1H-indol-2-yl)carbonyl]amino}phenyl)thieno[3,2-c]pyridine-7-carboxylic acid (1.0 g, 2.1 mmol) and 2,2-dimethoxy-1-ethanamine (252 uL, 2.3 mmol) were reacted according to General Procedure D. MP-carbonate resin (5 g) was added, and the mixture was shaken for 2 hours. The resin was filtered from the mixture and the filtrate was concentrated in vacuo to yield 1.5 g crude material. Isopropyl alcohol (35 mL) was added and the crude product was triturated and filtered to yield the title compound (830 mg, 71% yield): 1H NMR (DMSO, 400 MHz) δ 9.48 (s, 1H), 8.56 (s, 2H), 7.98 (d, 1H), 7.69 (d, 1H), 7.56-7.58 (m, 2H), 7.31-7.33 (m, 2H), 7.04-7.17 (m, 3H), 4.54 (t, 1H), 4.02 (s, 3H), 3.89 (s, 3H), 3.37 (t, 2H), 3.31 (s, 6H), 2.51 (t, 2H); RP-HPLC (Conditions j) Rt 12.2 min. MS: 560.0 MH+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07737160B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-48bd387e69e544afa47b3d3f5b1b5535 |
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| Quellennotiz | uspto-grants-2010_06 |
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