HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(7-(4-amino-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)-N-methylbenzamide → 4-(7-(2-Fluoro-4-(1-(4-fluorophenyl)-6-oxo-1,6-dihydropyridazine-5-carboxamido)phenoxy)thieno[3,2-b]pyridin-2-yl)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(7-(4-amino-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)-N-methylbenzamide | HCID 67348698 | — |
| Reactant | 1-((4-Fluorophenyl)carbamoyl)cyclopropanecarbonyl fluoride | HCID 86614649 | — |
| Reactant | 2-(4-Fluorophenyl)-3-oxo-2,3-dihydropyridazine-4-carbonyl fluoride | HCID 86614653 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(7-(2-Fluoro-4-(1-(4-fluorophenyl)-6-oxo-1,6-dihydropyridazine-5-carboxamido)phenoxy)thieno[3,2-b]pyridin-2-yl)benzoic acid | HCID 67345297 | — |
Reaction Steps
Prepared according to the procedure for Example 112, Step B substituting 4-(7-(4-amino-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)benzoic acid (1.25 g, 3.29 mmol) for 4-(7-(4-amino-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)-N-methylbenzamide and 2-(4-fluorophenyl)-3-oxo-2,3-dihydropyridazine-4-carbonyl fluoride (1.70 g, 5.75 mmol) for 1-((4-fluorophenyl)carbamoyl)cyclopropanecarbonyl fluoride. When the reaction was complete, water (20 mL) was added and the product (1.59 g, 80%) was collected by filtration to get a brown solid. LRMS (esi+) 597 m/z (M+1) detected.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08003662B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-ac1e1f7b52174f83a83d7153cffcfe2a |
| Source note | uspto-grants-2011_08 |