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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911883Generated: October 31, 2026

1,2-Dichloroethane → tert-Butyl 3-(1-Pivaloyl-1H-indazol-5-ylamino)piperidine-1-carboxylate

https://huagongshe.com/reaction/1911883

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantTert-butyl 3-oxopiperidine-1-carboxylateHCID 2756825—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 66716091HCID 66716091—
SolventSodium BicarbonateHCID 516892—
Producttert-Butyl 3-(1-Pivaloyl-1H-indazol-5-ylamino)piperidine-1-carboxylateHCID 5979978891%

Reaction Conditions

Temperature20 °C

Reaction Steps

Into a 1 L 3-neck round bottom flask fitted with a nitrogen inlet and mechanical stirrer was added tert-butyl 3-oxopiperidine-1-carboxylate (14.2 g, 0.07 mol), 1,2-dichloroethane (300 mL), and 1-(5-amino-1H-indazol-1-yl)-2,2-dimethylpropan-1-one maleate salt (23.0 g, 0.07 mol). The vessel was purged with nitrogen and stirred at 20° C. for one hour. Sodium triacetoxyborohydride (19.0 g, 0.09 mol) was added, and the reaction was monitored by analytical TLC to completion. The reaction was diluted with 100 mL of saturated sodium bicarbonate. The organic phase was isolated, dried over MgSO4, filtered and evaporated to dryness to afford the title compound as a yellow solid (25.0 g, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604205B2
Source datasetuspto-grants-2013_12
ORD IDord-7b1119ce6cbf40119ac231c27a8cb67d
Source noteuspto-grants-2013_12