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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931762Generated: November 5, 2026

Triethylamine → HCID 57965034, compound

https://huagongshe.com/reaction/1931762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(4-methanesulfonyl-phenoxy)-1-piperidin-4-yl-1H-pyrazolo[3,4-d]pyrimidine trifluoroacetate saltHCID 66915326—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 57965034HCID 57965034—

Reaction Steps

1-[1-(4-Fluoro-benzyl)-piperidin-4-yl]-4-(4-methanesulfonyl-phenoxy)-1H-pyrazolo[3,4-d]-pyrimidine was prepared according to General Procedure H by the reaction 4-(4-methanesulfonyl-phenoxy)-1-piperidin-4-yl-1H-pyrazolo[3,4-d]pyrimidine trifluoroacetate salt (Intermediate 27) with 4-fluorobenzaldehyde (available from Aldrich Chemical Company, Inc., Milwaukee, Wis., USA), triethylamine, and sodium triacetoxyborohydride in 1,2-dichloroethane. 1H NMR (400 MHz, DMSO-d6) δ 1.93-1.99 (m, 2H), 2.20-2.30 (m, 4H), 2.93-2.97 (m, 2H), 3.30 (methyl sulfonyl and water peak), 3.53 (s, 2H), 4.75-4.81 (m, 1H), 7.14-7.19 (m, 2H), 7.36-7.40 (m, 2H), 7.62-7.64 (m, 2H), 8.04-8.06 (m, 2H), 8.38 (s, 1H), 8.55 (s, 1H). Mass spectrum MH+=482.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188098B2
Source datasetuspto-grants-2012_05
ORD IDord-f19f5784d56543748bd03db1084ef05e
Source noteuspto-grants-2012_05