HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromoacetonitrile → HCID 24775759, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromoacetonitrile | HCID 11534 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 86618251 | HCID 86618251 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 24775759 | HCID 24775759 | 7% |
Reaction Steps
To a solution of tert-Butyl 4-{[5-hydroxy-1-(phenylsulfonyl)-1H-indol-4-yl]methyl}piperazine-1-carboxylate (45 mg, 0.10 mmol; Intermediate 64) in dry DCM (2 mL) was added bromoacetonitrile, 57 mg (0.48 mmol), tetrabutylammonium hydrogensulphate, 8 mg (0.02 mmol), 2M NaOH (1 mL) and the two phase system was vigorously stirred at room temperature over night. The organic phase was separated and the aqueous phase was washed once with water. The solvent from the combined organic phases was removed at reduced pressure and the residue was purified on a on a preparative HPLC, method B, to yield 2.9 mg (7%) of the target compound as a light brown oil. MS (ESI+) for C21H22N4O3S m/z 411 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07812017B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-a6222f6a08ce435cbb9849f69da1d87f |
| Source note | uspto-grants-2010_10 |