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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401899Generated: October 30, 2026

Methanol → HCID 66747529, compound

https://huagongshe.com/reaction/2401899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 66748126HCID 66748126—
SolventTetrahydrofuranHCID 8028—
SolventMethanol--water (1/1)HCID 22242641—
ProductHCID 66747529HCID 6674752992.2%

Reaction Steps

Methyl 4-cyano-5-(morpholin-4-yl)-3-[(4-oxoquinazolin-3(4H)-yl)methyl]thiophene-2-carboxylate (0.139 g, 0.339 mmol) was dissolved in Tetrahydrofuran (15.0 mL), Water (2.0 mL) and Methanol (5.0 mL). 1.00 M of Sodium hydroxide in Water (1.0 mL, 1.0 mmol) was added and the homogeneous solution was stirred at room temperature for 24 hours. The solution was concentrated in rotavapor to give a white crude solid, dissolved in H2O/MeOH (1/10, ˜20 mL) and concentrated in rotavapor until a white suspension (˜2 mL volume). The suspension was filtered to collect the solid, dried in lypholizer to give a white solid product (0.132 g, yield 92.2%). LC/MS: (FA) ES+ 397; ES− 395. 1H NMR (400 MHz, d4-methanol) δ 8.37 (s, 1H), 8.22 (d, J=8.03 Hz, 1H), 7.78-7.82 (m, 1H), 7.65 (d, J=7.28 Hz, 1H), 7.51-7.55 (m, 1H), 5.99 (s, 2H), 3.78-3.81 (m, 4H), 3.47-3.50 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796268B2
Source datasetuspto-grants-2014_08
ORD IDord-9ffbc306574c4312a9e568c5f393a8af
Source noteuspto-grants-2014_08