Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047560Generated: October 31, 2026

4-(2-(5-Nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-3-yl)-1H-benzo[d]imidazol-6-yl)morpholine → HCID 178507237, compound

https://huagongshe.com/reaction/1047560

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-(5-Nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-3-yl)-1H-benzo[d]imidazol-6-yl)morpholineHCID 136352261—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 178507237HCID 17850723753.8%

Reaction Steps

4-(2-(5-Nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-3-yl)-1H-benzo[d]imidazol-6-yl)morpholine (50 mg, 0.111 mmol) was added to the 10% Pd/C (10 mg) in ethanol (20 mL) and then hydrogen gas (60 psi) was applied for overnight at room temperature. Upon The reaction mixture was filtered through Celite, and the solvent was removed in vacuum. Purification by flash chromatography (5% CH3OH/CH2Cl2) afforded the title compound (25 mg) as a solid. 1H NMR: (400 MHz, CD3OD): δ 7.66 (d, 1H, J=2.4 Hz), 7.56-7.51 (m, 2H), 7.15 (m, 1H), 7.06-7.01 (m, 2H), 5.81 (dd, 1H, J=2.4 and 9.6 Hz), 4.01 (m, 1H), 3.87 (m, 4H), 3.81 (m, 1H), 3.65 (t, 1H, J=6.8 Hz), 3.16 (m, 4H), 2.67-2.58 (m, 1H), 2.16 (m, 1H), 2.08 (m, 1H), 1.84 (m, 1H), 1.69 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569511B2
Source datasetuspto-grants-2013_10
ORD IDord-a495738879474b2f9e21fe0bf3cf7c0a
Source noteuspto-grants-2013_10