HuagongsheHuagongshe Chemistry Print Report · For research reference only
Urea → 1-Benzyl-3-phenylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Urea | HCID 1176 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | Cyanoacetic acid | HCID 9740 | — |
| Reactant | HCID 2823049 | HCID 2823049 | — |
| Reactant | HCID 22922029 | HCID 22922029 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Product | 1-Benzyl-3-phenylurea | HCID 280363 | — |
Reaction Steps
N-Benzyl-N'-phenylurea was prepared preliminarily from phenyl isocyanate and benzylamine by the same procedure as in Reference Example 1. The urea compound as the starting material was reacted with cyanoacetic acid to form a uracil ring. Using sodium nitrite a nitroso group was introduced into the 5-position of the uracil ring in the obtained 6-amino-3-benzyl-1-phenyluracil and then reduced with hydrogen gas to prepare 3-benzyl-5,6-diamino-1-phenyluracil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05661153 |
| Source dataset | uspto-grants-1997_08 |
| ORD ID | ord-c92e178cab9f42eaa0e5287229d6ae66 |
| Source note | uspto-grants-1997_08 |