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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641957Generated: October 31, 2026

Sodium Hydroxide → 4-methyl-3-[6-(4-(2-methoxyethyl)piperazin-1-yl)-4-oxoquinazolin-3(4H)-yl]benzoic acid

https://huagongshe.com/reaction/641957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactantmethyl 4-methyl-3-[6-(4-(2-methoxyethyl)piperazin-1-yl)-4-oxoquinazolin-3(4H)-yl]benzoateHCID 68603298—
Product4-methyl-3-[6-(4-(2-methoxyethyl)piperazin-1-yl)-4-oxoquinazolin-3(4H)-yl]benzoic acidHCID 68603274—

Reaction Steps

Using an analogous procedure to that described paragraph (C) in the portion of Example 1 which is concerned with the preparation of starting material methyl 4-methyl-3-[6-(4-(2-methoxyethyl)piperazin-1-yl)-4-oxoquinazolin-3(4H)-yl]benzoate was hydrolysed with 1N NaOH to give 4-methyl-3-[6-(4-(2-methoxyethyl)piperazin-1-yl)-4-oxoquinazolin-3(4H)-yl]benzoic acid; NMR Spectrum: (DMSOd6) 2.16 (s, 3H), 3.30 (m, 9H), 3.60 (m, 2H), 3.80 (m, 2H), 4.00 (m, 2H), 7.58 (m, 2H), 7.69 (m, 2H), 7.93 (s, 1H), 8.00 (d, 1H), 8.16 (s, 1H), 11.07 (s, 1H), 13.10 (s, 1H); Mass Spectrum: M+H+ 423.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696215B2
Source datasetuspto-grants-2010_04
ORD IDord-91519e2cf0034e478aa1ff0ef72d0251
Source noteuspto-grants-2010_04