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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241423Generated: November 3, 2026

tert-Butyl (3S,4S)-4-amino-3-fluoropiperidine-1-carboxylate → (3S*,4S*)-tert-butyl 4-(1-(4-methoxybenzyl)-4-(4-amino-2-fluorophenoxy)-1H-pyrazolo[3,4-b]pyridin-3-ylamino)-3-fluoropiperidine-1-carboxylate

https://huagongshe.com/reaction/2241423

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl (3S,4S)-4-amino-3-fluoropiperidine-1-carboxylateHCID 57415840—
Reactant3-Fluoro-4-((3-iodo-1-(4-methoxybenzyl)-1H-pyrazolo[3,4-b]pyridin-4-yl)oxy)anilineHCID 67221003—
Product(3S*,4S*)-tert-butyl 4-(1-(4-methoxybenzyl)-4-(4-amino-2-fluorophenoxy)-1H-pyrazolo[3,4-b]pyridin-3-ylamino)-3-fluoropiperidine-1-carboxylateHCID 68509729—

Reaction Steps

Prepared from 4-(1-(4-methoxybenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridin-4-yloxy)-3-fluorobenzenamine (0.123 g, 0.25 mmol, prepared according to Example 7, Step B), and ±(3S*,4S*)-tert-butyl 4-amino-3-fluoropiperidine-1-carboxylate (0.164 g, 0.750 mmol, prepared according to the procedure described in WO 2006/087543) according to the procedure described for Example 143, Step A. LRMS (APCI+): m/z 581 (M+1) detected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723330B2
Source datasetuspto-grants-2010_05
ORD IDord-110a23858e2e458aaed56eb4dda06650
Source noteuspto-grants-2010_05