HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Sulfamic Acid → 3-(Cyclopropylmethoxy)-4-(difluoromethoxy)benzoic Acid
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Sulfamic Acid | HCID 5987 | — |
| Edukt | Chlorodifluoromethane | HCID 6372 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 3-(Cyclopropylmethoxy)-4-(difluoromethoxy)benzaldehyde | HCID 18973698 | — |
| Edukt | Sodium Chlorite | HCID 23668197 | — |
| Edukt | 3-(Cyclopropylmethoxy)-4-hydroxybenzaldehyde | HCID 71302977 | — |
| Katalysator | Benzyltrimethylammonium chloride | HCID 5963 | — |
| Produkt | 3-(Cyclopropylmethoxy)-4-(difluoromethoxy)benzoic Acid | HCID 2394006 | — |
Reaktionsschritte
In WO9501338 the reaction of 3-(cyclopropylmethoxy)-4-hydroxy-benzaldehyde with chlorodifluoromethane in the presence of sodium hydroxide and benzyl-trimethylammonium chloride (BTMA) in dioxane/water leads to 3-(cyclopropylmethoxy)-4-(difluoromethoxy)-benzaldehyde, which by oxidation with sodium chlorite and sulphamic acid yields 3-(cyclopropylmethoxy)-4-(difluoromethoxy)-benzoic acid. Chlorination of this acid with thionyl chloride in reflux toluene provides the corresponding acyl chloride, which is finally condensed with 3,5-dichloropyridine-4-amine in the presence of sodium hydride in tetrahydrofuran to thus reach roflumilast (I). These procedures are set out in Scheme 1.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09321726B2 |
| Quelldatensatz | uspto-grants-2016_04 |
| ORD ID | ord-44521b88145e401fb7e3c0db6db891fd |
| Quellennotiz | uspto-grants-2016_04 |