HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formamide → 2-[4-[4-(Pyrimidin-4-yl)phenoxy]butyl]-1H-isoindole-1,3(2H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formamide | HCID 713 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N,N',N''-Methylidynetrisformamide | HCID 78505 | — |
| Reactant | 2-[4-(4-Acetylphenoxy)butyl]-1H-isoindole-1,3(2H)-dione | HCID 67598087 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[4-[4-(Pyrimidin-4-yl)phenoxy]butyl]-1H-isoindole-1,3(2H)-dione | HCID 67599506 | — |
Reaction Steps
A mixture of 10.0 g of 2-[4-(4-acetylphenoxy]-butyl]-1H-isoindole-1,3(2H)-dione (Example 42) 10.0 g of tris(formamido)methane, and 20 ml of formamide are combined and the mixture stirred and heated at 160°-165° C. for 8 hours. After dilution with 100 ml of water, the mixture is rendered basic with 10N NaOH, the precipitate collected, washed with water, and air dried. Recrystallization from ethanol gives the pure compound, m.p. 100°-102° C.; yield, 5.0 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05877196 |
| Source dataset | uspto-grants-1999_03 |
| ORD ID | ord-14a0374f1cf0424bb6cd26c83a98c3ef |
| Source note | uspto-grants-1999_03 |