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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159811Generated: November 3, 2026

Bromoacetonitrile → HCID 24775759, compound

https://huagongshe.com/reaction/1159811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetonitrileHCID 11534—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 86618251HCID 86618251—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventDichloromethaneHCID 6344—
ProductHCID 24775759HCID 247757597%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812017B2
Source datasetuspto-grants-2010_10
ORD IDord-a6222f6a08ce435cbb9849f69da1d87f
Source noteuspto-grants-2010_10