HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 7-Acetyl-4-(benzyloxy)-1,3-benzothiazol-2(3H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 7-Acetyl-4-hydroxybenzo[d]thiazol-2(3H)-one | HCID 45076987 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-Acetyl-4-(benzyloxy)-1,3-benzothiazol-2(3H)-one | HCID 69321983 | — |
Reaction Steps
To a solution of 7-acetyl-4-hydroxy-1,3-benzothiazol-2(3H)-one (153 mg), in dry THF (3 ml) and dry DMF (0.5 ml) under nitrogen, was added N,N-diisopropylethylamine (0.13 ml) and benzyl bromide (0.09 ml), and the mixture stirred for 72 h. Water (10 ml) was added and the mixture extracted with ethyl acetate. The organic phases were combined, washed with brine, dried (MgSO4), and evaporated in vacuo. The residue was purified on a 5 g silica SPE cartridge, eluting with a stepped gradient of 10% to 50% ethyl acetate-cyclohexane mixtures, to give the title compound (68 mg). LCMS RT=3.14 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07402598B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-b853c45fcafa4252a8f6ce0233d3b0e2 |
| Source note | uspto-grants-2008_07 |