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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552418Generated: November 1, 2026

1-benzyl-3-tert-butyl-1H-pyrazole-5-carbonyl chloride → HCID 45142431, compound

https://huagongshe.com/reaction/552418

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-benzyl-3-tert-butyl-1H-pyrazole-5-carbonyl chlorideHCID 2799322—
Reactant7-(3-aminophenoxy)-1H-imidazo[4,5-b]pyridin-2(3H)-oneHCID 45140141—
ProductHCID 45142431HCID 4514243139%

Reaction Steps

Method H was used with 7-(3-aminophenoxy)-1H-imidazo[4,5-b]pyridin-2(3H)-one and 1-benzyl-3-tert-butyl-1H-pyrazole-5-carbonyl chloride to afford the title compound (40 mg, 39%). 1H-NMR (δ, ppm, DMSO-d6): 1.29 (s, 9H, t-Bu), 5.67 (s, 2H, CH2), 6.47 (d, 1H, HPy,5, J=6.0 Hz), 6.89 (d, 1H, Harom, J=8.0 Hz), 7.00 (s, 1H, Hpyrrazole), 7.11 (d, 2H, Harom, J=8.0 Hz), 7.22 (t, 1H, Harom, J=7.0 Hz), 7.11 (t, 2H, Harom, J=8.0 Hz), 7.40 (t, 1H, Harom, J=8.0 Hz), 7.48-7.51 (m, 1H, Harom), 7.60 (d, 1H, Harom, J=8.0 Hz), 7.79 (d, 1H, HPy,6, J=6.0 Hz), 10.23 (s, 1H, NHamide), 11.18 (s, 1H, NHPy3), 11.38 (s, 1H, NHPy2). HRMS (EI): m/z [M+H] calcd for C27H27N6O3: 483.2145; found: 483.2145.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951819B2
Source datasetuspto-grants-2011_05
ORD IDord-b94891cb690e44799f97815e9103e243
Source noteuspto-grants-2011_05