HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylamine → S-1-(4-Fluorophenyl)-1H-indazol-5-yl benzothioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 3,4,7,8-Tetramethyl-1,10-phenanthroline | HCID 74265 | — |
| Reactant | 1-(4-fluorophenyl)-5-iodo-1H-indazole | HCID 59251128 | — |
| Reactant | HCID 178526132 | HCID 178526132 | — |
| Catalyst | HCID 178505377 | HCID 178505377 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | S-1-(4-Fluorophenyl)-1H-indazol-5-yl benzothioate | HCID 59339848 | 20% |
Reaction Steps
To a solution of 1-(4-fluorophenyl)-5-iodo-1H-indazole (103e, 0.224 g, 0.66 mmol), thiobenzoic acid (0.093 ml, 0.79 mmol), 3,4,7,8-tetramethyl-1,10-phenantroline (0.031 g, 0.13 mmol) and N,N-diisopropylamine (0.220 ml, 1.32 mmol) in toluene (2.5 ml) was added copper(I) iodine (2.245 μl, 0.07 mmol). The resulting mixture was stirred at 110 C O/N. The reaction mixture was cooled to r.t. diluted with EtOAc and washed with water. The organic phase was the dried the solvent evaporated and then purified on HPLC. The relevant fractions were collected freeze dried to give 45 mg of product (20% yield) which was analysed by LC/MS.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08143290B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-13e8d4e2deb84cf195674b757c3d3977 |
| Source note | uspto-grants-2012_03 |