HuagongsheHuagongshe Chemistry Print Report · For research reference only
Borohydride → HCID 58828971, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Borohydride | HCID 28123 | — |
| Reactant | HCID 58828974 | HCID 58828974 | — |
| Reactant | HCID 178442555 | HCID 178442555 | — |
| Solvent | Tetrahydrofuran ethanol | HCID 21873804 | — |
| Product | HCID 58828971 | HCID 58828971 | — |
Reaction Steps
2.647 g (6.62 mmol, 3 eq) of resin-supported borohydride and 30 mg (0.06 mmol, 0.03 eq) of bis(bipyridine)dibromonickel (II) are added to a solution of 0.706 g (3.31 mmol, 1.5 eq) of 5-heptyl-4-methyl-4H-[1,2,4]-triazole-3-thiol in 10 ml of tetrahydrofuran/ethanol 5/5. To the suspension obtained there is added a solution of 100 mg (0.22 mmol, 1 eq) of ethyl [4-(4-iodo-2-propoxybenzylamino)phenyl]acetate in 10 ml of tetrahydrofuran/ethanol 5/5. The reaction mixture is stirred overnight under reflux. After returning to room temperature, the reaction medium is filtered, concentrated and then chromatographed on silica gel (heptane/ethyl acetate 40/60). After evaporation of the solvents, 0.750 g (63%) of the expected compound is recovered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07829588B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-451756e1e3eb4ffaa47f27b4a5a7d69c |
| Source note | uspto-grants-2010_11 |