HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Isobutylamine → 7-amino-2,2-dimethyl-8-(2-methylpropyl)-6-nitroso-3H-imidazo[1,2-a]pyrimidin-5-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Isobutylamine | HCID 6558 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 4-Chlorobenzylamine | HCID 66036 | — |
| Edukt | Sodium dithionate | HCID 146045 | — |
| Edukt | Ethyl 2-cyano-2-(hydroxyimino)acetate | HCID 6399078 | — |
| Edukt | HCID 178448423 | HCID 178448423 | — |
| Edukt | 2-Methylthio-4,4-dimethyl-2-imidazoline hydrochloride | HCID 178503443 | — |
| Lösungsmittel | Formic Acid | HCID 284 | — |
| Produkt | 7-amino-2,2-dimethyl-8-(2-methylpropyl)-6-nitroso-3H-imidazo[1,2-a]pyrimidin-5-one | HCID 178448424 | — |
Reaktionsschritte
6,7-DIHYDRO-4-(2-METHYLPROPYL)-6,6-DIMETHYL-3H-IMIDAZO[1,2-a]PURIN-9(4H)-ONE.- 7-Amino-2,3-dihydro-2,2-dimethyl-8-(2-methylpropyl)-6-nitrosoimidazo[1,2-a]pyrimidin-5(8H)-one was prepared by reaction of the 2-methylthio-4,4-dimethyl-2-imidazoline hydrochloride with 2-methylpropylamine according to the method of Procedure 103 by substitution of the latter for p-chlorobenzylamine. The reaction product from this step was then condensed with ethyl oximinocyanoacetate as described in Procedure 103. The resulting nitroso compound was then reduced with sodium dithionate in formic acid and the resulting formylamino compound was cyclized with dilute aqueous sodium hydroxide according to Procedure 100.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04404380 |
| Quelldatensatz | uspto-grants-1983_09 |
| ORD ID | ord-7304ffcd44004157ba9f1297dac79bb2 |
| Quellennotiz | uspto-grants-1983_09 |