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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931611Generated: November 4, 2026

Trifluoroacetic acid → HCID 57964985, compound

https://huagongshe.com/reaction/1931611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantIsopropyl chloroformateHCID 7917—
Reactant4-[4-(4-Methanesulfonyl-phenylamino)-pyrazolo[3,4-d]pyrimidin-1-yl]-piperidine-1-carboxylic acid tert-butyl esterHCID 53257791—
ProductHCID 57964985HCID 57964985—

Reaction Steps

4-[4-(4-Methanesulfonyl-phenylamino)-pyrazolo[3,4-d]pyrimidin-1-yl]-piperidine-1-carboxylic acid isopropyl ester was prepared according to General Procedure D by the reaction of 4-[4-(4-methanesulfonyl-phenylamino)-pyrazolo[3,4-d]pyrimidin-1-yl]-piperidine-1-carboxylic acid tert-butyl ester (Example 5) with trifluoroacetic acid, followed by reaction of the resulting amine with isopropyl chloroformate (available from Aldrich Chemical Company, Inc., Milwaukee, Wis., USA). 1H NMR (400 MHz, DMSO-d6) δ 1.20 (d, 6H, J=6.2 Hz), 1.95-2.01 (m, 4H), 2.98-3.09 (m, 2H), 3.19 (s, 3H), 4.07-4.12 (m, 2H), 4.78-4.82 (m, 1H), 4.93-4.97 (m, 1H), 7.92-7.94 (m, 2H), 8.17-8.19 (m, 2H), 8.41 (s, 1H), 8.54 (s, 1H), 10.49 (s, 1H). Mass spectrum MH+=459.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188098B2
Source datasetuspto-grants-2012_05
ORD IDord-cb824c15407644fe86daf698a0a11ed3
Source noteuspto-grants-2012_05