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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173248Generated: October 30, 2026

Sodium Thiosulfate → 5-fluoro-1-(piperazin-1-ylmethyl)-2,3-dihydro-1H-indene-4-carbonitrile

https://huagongshe.com/reaction/2173248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant5-fluoro-1-(hydroxymethyl)-2,3-dihydro-1H-indene-4-carbonitrileHCID 66646390—
CatalystAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Product5-fluoro-1-(piperazin-1-ylmethyl)-2,3-dihydro-1H-indene-4-carbonitrileHCID 59568675—

Reaction Steps

A solution of 5-Fluoro-1-(hydroxymethyl)-2,3-dihydro-1H-indene-4-carbonitrile (20 mg, 0.105 mmol) in DCM was treated with Dess-MartinPeriodinane (89 mg, 0.209 mmol) in DCM. When TLC showed the reaction was done, Na2S2O3 was added to the reaction. The solution was stirred vigorously until the two layers turned clear. The mixture was extracted with DCM, and the DCM layer was washed with Na2CO3 and brine, dried over sodium sulfate, and concentrated. The resulting oil was then treated with N-Boc-piperazine (39.0 mg, 0.209 mmol) and Sodium Cyanoborohydride (33 mg, 0.52 mmol) in DCM with a few drops of HOAc. LC showed complete reaction within 6 hours. The reductive amination adduct was then purified by MPLC. Finally, the Boc group was removed by treating the carbamate with 4N HCl in dioxane. After removal of solvent, the title material was obtained. LC-MS (IE, m/z): 260 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056859B2
Source datasetuspto-grants-2015_06
ORD IDord-9663b0f686b247068322e49d3e55e2fa
Source noteuspto-grants-2015_06