Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354237Generated: October 30, 2026

Methanesulfonic Acid → HCID 86610965, compound

https://huagongshe.com/reaction/2354237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantHCID 11374246HCID 11374246—
SolventEthyl AcetateHCID 8857—
ProductHCID 86610965HCID 86610965—

Reaction Steps

Using an analogous procedure to that described in Example 45, 1N methanesulfonic acid in ethyl acetate was reacted with N-cyclopropyl-3-[6-{[(3S)-1-isopropylpyrrolidin-3-yl]oxy}-4-oxoquinazolin-3(4H)-yl]-4-methylbenzamide to gave the title compound; NMR Spectrum: (DMSOd6) 0.56 (m, 2H), 0.70 (m, 2H), 1.30 (m, 6H), 2.14 (s, 3H), 2.26 (m, 1H), 2.36 (s, 3H), 2.85 (m, 1H), 3.27-4.00 (m, 6H), 5.38 (m, 1H), 7.54 (d, 1H), 7.58 (d, 1H), 7.63 (s, 1H), 7.80 (d, 1H), 7.84 (s, 1H), 7.91 (d, 1H), 8.23 (s, 1H), 8.45 (m, 1H), 9.95 (br d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750154B2
Source datasetuspto-grants-2010_07
ORD IDord-cae97fd9b35c47548bd14e7bcebf86f3
Source noteuspto-grants-2010_07