HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(2-aminoethyl)acetamide → N-[2-(2-chloro-5-iodopyrimidine-4-ylamino)ethyl]acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(2-aminoethyl)acetamide | HCID 66082 | — |
| Reactant | 2,4-Dichloro-5-iodopyrimidine | HCID 263438 | — |
| Product | N-[2-(2-chloro-5-iodopyrimidine-4-ylamino)ethyl]acetamide | HCID 59550867 | 71% |
Reaction Steps
In the reaction of 2,4-dichloro-5-iodopyrimidine (1.0 g, 3.6 mmol) with N-(2-aminoethyl)acetamide (e. g. ABCR, Aldrich) (0.42 mL, 3.9 mmol) according to procedure 2, the desired product is obtained in 71% yield (878 mg) after trituration of the crystals obtained with diethyl ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07825128B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-9b50b58ab8894daf9a8b50c2a62e9fc8 |
| Source note | uspto-grants-2010_11 |