HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenemethanamine, 4-chloro-N-methyl- → HCID 57619453, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenemethanamine, 4-chloro-N-methyl- | HCID 66905 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,4-Dichloro-1,3-thiazole-5-carboxaldehyde | HCID 1488672 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57619453 | HCID 57619453 | 119,525.203% |
Reaction Steps
To a solution of (4-chloro-benzyl)-methyl-amine (550, 2 g, 0.01 mol) and N,N-diisopropylethylamine (4 mL, 0.03 mol) in tetrahydrofuran (50 mL) was added 2,4-dichloro-thiazole-5-carbaldehyde (93, 3 g, 0.01 mmol) in tetrahydrofuran (20 mL) at room temperature. The reaction mixture was stirred at room temperature overnight. The reaction mixture was poured into ice water, extracted with ethyl acetate, washed with brine, and dried over sodium sulfate. After removal of solvent, the residue was collected by filtration and washed with hexanes to provide the desired compound as a light-yellow solid (551, 3.6 g, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09169250B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-fd928a00dbf249068e1904ba5841c612 |
| Source note | uspto-grants-2015_10 |