HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 2-(4,5-Dihydro-1,3-thiazol-2-yl)-N-methyl-1H-indole-7-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 2-(4,5-Dihydro-1,3-thiazol-2-yl)-1H-indole-7-amine | HCID 57901777 | — |
| Reactant | HCID 178418385 | HCID 178418385 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4,5-Dihydro-1,3-thiazol-2-yl)-N-methyl-1H-indole-7-amine | HCID 57901587 | 31.3% |
Reaction Steps
2-(4,5-Dihydro-1,3-thiazol-2-yl)-1H-indole-7-amine (1.08 g), aqueous formaldehyde solution (37%, 372 μL) and benzotriazole (595 mg) were dissolved in ethanol (15 mL) and tetrahydrofuran (15 mL), and the mixture was stirred at room temperature for 2 days. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The obtained residue was subjected to silica gel column chromatography (ethyl acetate:hexane=1:1) to give a yellow oil (360 mg, yield 31%). M+1=232.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08957070B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-f409d5ed5b564901aa42b152017630bb |
| Source note | uspto-grants-2015_02 |