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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451606Generated: October 29, 2026

HCID 11305064, compound → N-1H-indazol-4-yl-N'-(5-piperidin-1-yl-2,3-dihydro-1H-inden-1-yl)urea

https://huagongshe.com/reaction/451606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11305064HCID 11305064—
ReactantHCID 22927197HCID 22927197—
ProductN-1H-indazol-4-yl-N'-(5-piperidin-1-yl-2,3-dihydro-1H-inden-1-yl)ureaHCID 11428814—

Reaction Steps

The title compound was prepared using the procedure in Example 9, except using methyl 4-({[(5-piperidin-1-yl-2,3-dihydro-1H-inden-1-yl)amino]carbonyl}amino)-1H-indazole-1-carboxylate instead of methyl 4-({[5-tert-butyl-2,3-dihydro-1H-inden-1-yl]amino}carbonyl)amino]-1H-indazole-1-carboxylate. 1H NMR (DMSO-d6) δ 1.09 (t, 1.2H, Et2O), 1.40-2.20 (br m, 7H), 2.52-2.59 (m, 1H), 2.84-2.96 (m, 1H), 2.96-3.07 (m, 1H), 3.38 (q, 0.8H, Et2O), 3.52 (m, 4H), 5.24 (m, 1H), 5.76 (s, 0.2H, CH2Cl2), 7.05 (d, 1H), 7.21 (m, 1H), 7.33 (m, 1H), 7.50 (d, 1H), 7.65-7.77 (m, 3H), 8.29 (s, 1H), 9.15 (s, 1H); MS (ESI+) 376 (M+H)+; Elemental: Calculated for C22H25N5O.2HCl.0.1CH2Cl2-0.2Et2O: C58.31, H6.24, N14.85; Found: C58.22, H6.54, N15.00.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08487116B2
Source datasetuspto-grants-2013_07
ORD IDord-71821c4f753946108df15f736ff2ef96
Source noteuspto-grants-2013_07