HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetamidine → N-((4-Amino-2-methyl-5-pyrimidinyl)methyl)formamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetamidine | HCID 67171 | — |
| Reactant | alpha-Methoxymethylene-beta-formylaminopropionitrile | HCID 54062148 | — |
| Product | N-((4-Amino-2-methyl-5-pyrimidinyl)methyl)formamide | HCID 597195 | — |
Reaction Steps
The α-methoxymethylene-β-formylaminopropionitrile solution and the acetamidine solution are combined. The mixture is reacted at 25°C for 10 minutes. The reaction mixture is subjected to concentration at not higher than 40°C to give crystals. The produced crystals are washed with 50 parts by volume of ethanol, whereby 24.8 parts of 2-methyl-4-amino-5-formylaminomethylpyrimidine is obtained as crystals (Purity: 93 %). The ethanol washing is concentrated to give 16 parts of 2-methyl-4-amino-5-formylaminomethylpyrimidine as crystals (Purity: 47.5 %).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03954756 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-ba9435c8b58f426881a6b2e81a6aeee9 |
| Source note | uspto-grants-1976_05 |