Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1853405Generated: October 25, 2026

3-Amino-2-phenyl-4(3H)-quinazolinone → 3-(1-adamantyl)-N-(4-oxo-2-phenylquinazolin-3(4H)-yl)propanamide

https://huagongshe.com/reaction/1853405

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-2-phenyl-4(3H)-quinazolinoneHCID 722876—
Reactant3-(1-Adamantyl)propanoyl chlorideHCID 15533306—
Product3-(1-adamantyl)-N-(4-oxo-2-phenylquinazolin-3(4H)-yl)propanamideHCID 49872536—

Reaction Steps

3-Amino-2-phenyl-4(3H)-quinazolinone and the product of Example 13A were reacted as described in Example 5 to provide the title compound. 1H NMR (300 MHz, DMSO-d6) δ ppm 0.93-1.13 (m, 2H), 1.23-1.33 (m, 6H), 1.51-1.65 (m, 6H), 1.85-1.89 (m, 3H), 1.96-2.08 (m, 2H), 7.44-7.55 (m, 3H), 7.58-7.64 (m, 3H), 7.75 (d, J=7.8 Hz, 1H), 7.89-7.94 (m, 1H), 8.18 (dd, J=8.0, 1.2 Hz, 1H), 11.06 (s, 1H) ppm; MS (DCI/NH3) m/z 428 (M+H)+; Elemental Analysis: Calculated for C27H29N3O2: C, 75.85; H, 6.84; N, 9.83. Found: C, 75.75; H, 6.97; N, 9.84.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962639B2
Source datasetuspto-grants-2015_02
ORD IDord-b3d71d1180994b728fbba986b7c0404a
Source noteuspto-grants-2015_02