HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2,6-Dichloro-5-nitropyrimidin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,4,6-Trichloro-5-nitropyrimidine | HCID 4297843 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,6-Dichloro-5-nitropyrimidin-4-amine | HCID 350811 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A solution of 2,4,6-trichloro-5-nitropyrimidine (94 mg, 0.413 mmol) in THF (5 mL) was cooled to −78° C. and treated with Et3N (110 μL, 0.757 mmol), followed by NH3 (7 N in MeOH, 50 μL, 0.344 mmol). The reaction was warmed to 0° C. Once TLC indicated complete consumption of the starting material, the crude product solution was immediately used in the reaction below (Scheme 40).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08629142B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-78d78ece27574972ab7b607ff3724d01 |
| Source note | uspto-grants-2014_01 |