HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2,6-Dichloropyrimidine-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,6-dichloropyrimidine-4-carbonyl Chloride | HCID 11031133 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2,6-Dichloropyrimidine-4-carboxamide | HCID 241128 | 41.1% |
Reaction Steps
To a solution of 2,6-dichloropyrimidine-4-carbonyl chloride (26.13 g, 123.6 mmol) in Et2O (500 mL) was added a mixture of 0.5M ammonia in dioxane (250 mL, 125 mmol) and iPr2NEt (22 mL, 126 mmol) dropwise over approximately 50 minutes. After stirring overnight the reaction was concentrated in vacuo to a residue and chromatographed over silica gel with 10-50% EtOAc in hexanes. The product fractions were evaporated in vacuo, and the resulting solid residue triturated with 10 mL 10% EtOAc/hexanes and filtered to give 2,6-dichloropyrimidine-4-carboxamide as an orange crystalline solid (9.743 g, 50.74 mmol, 41% yield). LC/MS: m/z=192.2 [M+H]+, 1H NMR (400 MHz, DMSO-d6): 8.40 (1H, br s), 8.16 (1H, br s), 8.10 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09163008B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-ba80fda56709426fb6d2230b453c3d22 |
| Source note | uspto-grants-2015_10 |