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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746546Generated: October 29, 2026

alpha-Methyl-4-(2-methylpropyl)benzeneacetyl chloride → HCID 23381272, compound

https://huagongshe.com/reaction/746546

Reaction equation

Participants

RoleNameHCIDCharge
Reactantalpha-Methyl-4-(2-methylpropyl)benzeneacetyl chlorideHCID 595157—
Reactant1-(4-aminobutyl)-1H-imidazo[4,5-c]quinolin-4-amineHCID 15453775—
ProductHCID 23381272HCID 23381272—

Reaction Steps

According to the general method of Example 14, 1-(4-aminobutyl)-1H-imidazo[4,5-c]quinolin-4-amine and 4-isobutyl-α-methylphenylacetyl chloride were combined to provide N1-[4-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-2-(4-isobutylphenyl)propanamide as a white powder, m.p. 172.0-173.0° C. 1H NMR (300 MHz, DMSO-d6) δ 8.14 (s, 1H), 8.01 (d, J=7.6 Hz, 1H), 7.90 (t, J=5.6 Hz, 1H), 7.63 (dd, J=8.1, 1.0 Hz, 1H), 7.44 (dt, J=7.0, 1.0 Hz, 1H), 7.25 (dt, J=7.0 Hz, 1H), 7.14 (d, J=8.0 Hz, 2H), 6.97 (d, J=8.0 Hz, 2H), 6.58 (broad s, 2H), 4.55 (t, J=7.0 Hz, 2H), 3.47 (q, J=7.1 Hz, 1H), 3.06 (m, 2H), 2.34 (d, J=7.11 Hz, 2H), 1.80-1.69 (m, 3H), 1.44 (m, 2H), 1.24 (d, J=7.0 Hz, 3H), 0.82 (d, J=6.6 Hz, 6H); MS (EI) m/e 443.2687 (443.2685 calcd for C27H33N5O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07393859B2
Source datasetuspto-grants-2008_07
ORD IDord-dd2c9b8bd5ae44b59963aa70e1a78e66
Source noteuspto-grants-2008_07