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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1529856Generated: November 2, 2026

Piperidine → (R)-2-(3-(4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidine-1-carbonyl)-3-cyclopropylacrylonitrile

https://huagongshe.com/reaction/1529856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantCyclopropanecarboxaldehydeHCID 123114—
Reactant3-(3-(4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl)-3-oxopropanenitrileHCID 71015688—
SolventMethanolHCID 887—
Product(R)-2-(3-(4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidine-1-carbonyl)-3-cyclopropylacrylonitrileHCID 7101569365%

Reaction Steps

A mixture of 3-[3-[4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]piperidin-1-yl]-3-oxopropanenitrile (120 mg, 0.26 mmol, 1.00 equiv), piperidine (27 mg, 0.28 mmol, 1.07 equiv) and cyclopropanecarbaldehyde (28 mg, 0.40 mmol, 1.51 equiv) in methanol (8 mL) was stirred in sealed tube at room temperature for 24 h. The resulting mixture was concentrated under vacuum and the residue was purified on a silica gel column eluted with dichloromethane/methanol (100/1) to give 85.4 mg (64%) of the title compound as a white solid. MS (ESI, pos. ion) m/z: 506 (M+1). 1HNMR(300MHz,CDCl3, ppm) 8.392 (1H, s), 7.676˜7.581 (2H, t), 7.445˜7.393 (2H, t), 7.202˜7.097 (5H, m), 6.601˜6.566 (1H,d, J=10.5), 5.737(2H,s), 5.010˜4.912 (1H,m), 4.691˜3.185 (4H,m), 2.464˜2.035 (5H,m), 1.275˜0.876 (4H,m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090621B2
Source datasetuspto-grants-2015_07
ORD IDord-ddac5da174884a7d93150767411c9b20
Source noteuspto-grants-2015_07