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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55007Generated: October 25, 2026

1-Iodopropane → 3-[1-(6,7-Dimethoxy-4-quinazolinyl)-4-piperidinyl]-1,2,3,4-tetrahydro-6-nitro-2,4-dioxo-1-propyl-quinazoline

https://huagongshe.com/reaction/55007

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IodopropaneHCID 33643—
Reactant3-[1-(6,7-Dimethoxy-4-quinazolinyl)-4-piperidinyl]-1,2,3,4-tetrahydro-6-nitro-2,4-dioxoquinazolineHCID 22923399—
Product3-[1-(6,7-Dimethoxy-4-quinazolinyl)-4-piperidinyl]-1,2,3,4-tetrahydro-6-nitro-2,4-dioxo-1-propyl-quinazolineHCID 2292355664%

Reaction Steps

The procedure similar to that described in Example 1 was repeated, except that 300 mg (0.63 mmol) of Compound 24 was used and propyl iodide was used in place of methyl iodide. As a result, 209.9 mg (yield: 64%) of Compound 3 was obtained as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05624926
Source datasetuspto-grants-1997_04
ORD IDord-2533bc7685ed47bfaef9ea3d3763143b
Source noteuspto-grants-1997_04