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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592416Generated: November 1, 2026

tert-butyl 4-amino-1H-pyrazole-1-carboxylate → 2-(2-(2-(2-(1H-Pyrazol-4-ylamino)-5-chloropyrimidin-4-yl)ethyl)phenyl)propanamide

https://huagongshe.com/reaction/592416

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 4-amino-1H-pyrazole-1-carboxylateHCID 59587648—
Reactant2-(2-(2-(2,5-Dichloropyrimidin-4-yl)ethyl)phenyl)propanamideHCID 86712307—
SolventMethanol--water (1/1)HCID 22242641—
Product2-(2-(2-(2-(1H-Pyrazol-4-ylamino)-5-chloropyrimidin-4-yl)ethyl)phenyl)propanamideHCID 7329720652%

Reaction Steps

A solution of 2-(2-(2-(2,5-dichloropyrimidin-4-yl)ethyl)phenyl)propanamide A30 (0.10 g, 0.31 mmol) and tert-butyl 4-amino-1H-pyrazole-1-carboxylate (0.17 g, 0.93 mmol) was heated in MeOH:water (10:1, 5 mL) at 90° C. for 18 hours. The solvents were removed in vacuo and the crude residue was purified by silica gel column chromatography (Combiflash Rf, 0-15% MeOH in DCM). The purified fractions were combined, the solvent was removed in vacuo and the solid was sonicated in cyclohexane and filtered. The residue was dried in vacuo to give the title compound 35 as a light yellow solid (0.060 g, 52%). 1H NMR (300 MHz, d6-DMSO) δ 1.34 (d, J=7.04 Hz, 3H), 2.92-3.11 (m, 4H), 3.86 (q, J=7.04 Hz, 1H), 6.85 (brs, 1H), 7.13-7.25 (m, 4H), 7.36-7.44 (m, 1H), 7.57-87 (m, 2H), 8.37 (s, 1H), 9.63 (s, 1H). LCMS-C: rt 4.72 min; m/z 371 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238644B2
Source datasetuspto-grants-2016_01
ORD IDord-00e62413af124f9f8eafe4d7ebecbd43
Source noteuspto-grants-2016_01