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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354240Generated: November 1, 2026

Methanesulfonic Acid → HCID 86610968, compound

https://huagongshe.com/reaction/2354240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantHCID 11751183HCID 11751183—
SolventEthyl AcetateHCID 8857—
ProductHCID 86610968HCID 86610968—

Reaction Steps

Using an analogous procedure to that described in Example 45, two equivalents of 1N methanesulfonic acid in ethyl acetate was reacted with N-cyclopropyl-3-[6-(4-isopropylpiperazin-1-yl)-4-oxoquinazolin-3(4H)-yl]-4-methylbenzamide to gave the title compound; NMR Spectrum: (DMSOd6) 0.56 (m, 2H), 0.70 (m, 2H), 1.15 (m, 6H), 1.92 (s, 1H), 2.14 (s, 3H), 2.32 (s, 6H), 2.54 (m, 4H), 2.87 (m, 1H), 2.99 (m, 1H), 3.18 (m, 4H), 4.06 (m, 1H), 7.52 (m, 2H), 7.67 (s, 2H), 7.82 (d, 1H), 7.91 (m, 1H), 8.11 (s, 1H), 8.44 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750154B2
Source datasetuspto-grants-2010_07
ORD IDord-3a6a1b594d04401d99621f928516ec38
Source noteuspto-grants-2010_07