HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylhydrazine → 4-[(Aminooxy)methyl]-2-(hex-1-yn-1-yl)-1,3-thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | 2-{[2-(hex-1-yn-1-yl)-1,3-thiazol-4-yl]methoxy}-1H-isoindole-1,3(2H)-dione | HCID 67426046 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[(Aminooxy)methyl]-2-(hex-1-yn-1-yl)-1,3-thiazole | HCID 67425209 | 94% |
Reaction Steps
To a solution of 2-{[2-(hex-1-yn-1-yl)-1,3-thiazol-4-yl]methoxy}-1H-isoindole-1,3(2H)-dione (13.6 g, 40.1 mmol) in tetrahydrofuran (250 mL) was added methylhydrazine (3.69 g, 80.1 mmol) dropwise. After stirring 20 h at room temperature, the reaction mixture was concentrated in vacuo, diluted with ethyl acetate, washed with water and the organic layer drid (MgSO4) and concentrated in vacuo. Purification on silica gel afforded 4-[(aminooxy)methyl]-2-(hex-1-yn-1-yl)-1,3-thiazole as a colourless oil [8.15 g, yield 94%; HPLC/MS: m/z=211 (M+H); log P(HCOOH)=1.76].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08580799B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-24cda93e0fd5435eb71832abb805a278 |
| Source note | uspto-grants-2013_11 |