HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azetidine → 4-(Azetidin-1-yl)-6-chloropyrimidine-5-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azetidine | HCID 10422 | — |
| Reactant | 4,6-Dichloro-5-pyrimidinecarbaldehyde | HCID 819691 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-(Azetidin-1-yl)-6-chloropyrimidine-5-carbaldehyde | HCID 86712562 | — |
Reaction Steps
To a solution of 4,6-dichloropyrimidine-5-carbaldehyde (1.00 g, 5.65 mmol) in chloroform at 0° C. were added azetidine (99%, 0.392 mL, 5.71 mmol) and triethylamine (5 drops). The reaction mixture was allowed to warm to room temperature and then stirred for 18 hours. The reaction mixture was filtered, and the filtrate was purified by silica gel chromatography (Gradient: 0% to 100% ethyl acetate in heptane) to provide the product. Yield: 880 mg, 4.45 mmol, 79%. LCMS m/z 198.1, 200.1 (M+1). 1H NMR (400 MHz, CD3OD) δ 2.34-2.43 (m, 2H), 4.12-4.33 (br m, 4H), 8.30 (s, 1H), 10.28 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829010B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-50b2e28456f84a5494615235ad31a5bc |
| Source note | uspto-grants-2014_09 |