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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255540Generated: November 2, 2026

HCID 131718082, compound → HCID 131718081, compound

https://huagongshe.com/reaction/2255540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131718082HCID 131718082—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 131718081HCID 13171808167%

Reaction Steps

0.11 g (0.21 mmol) of 2-butyl-3-[(2'-(t-butoxycarbonyl)biphen-4-yl)methyl]-6-nitroquinazolin-3(1H)-one (Example 21) was suspended in 7.5 mL of MeOH and hydrogenated over 55 mg of 10% Pd/C under an atmospheric pressure hydrogen blanket. After 1 hour the reaction mixture was filtered through celite and the filtrate concentrated in vacuo. The residue was purified by flash chromatography over silica gel eluting with 50% EtOAc/hexane to give 69 mg (0.14 mmol) of a white foam, 67% yield. 1H-NMR (CDCl3): 0.94 (t, 3H, J=7. Hz), 1.23 (s, 9H), 1.41 (m, 2H), 1.79 (m, 2H), 2.74 (3 line m, 2H, J=7.7 Hz), 5.44 (bs, 2H), 7.05-7.57 (m, 10H), 7.77 (d, J=7.5 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05240928
Source datasetuspto-grants-1993_08
ORD IDord-a10b29c5446146beabeb96ccb6245441
Source noteuspto-grants-1993_08