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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291280Generated: October 30, 2026

Sodium Hydroxide → HCID 135667586, compound

https://huagongshe.com/reaction/1291280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant3-(4-Chlorobenzoyl)benzyl bromideHCID 13649653—
ReactantHCID 178430835HCID 178430835—
SolventMethanolHCID 887—
Solventdimethoxyethane N,N-dimethylformamideHCID 18463208—
ProductHCID 135667586HCID 13566758663.1%

Reaction Steps

In methanol (18.7 ml) was suspended 5-methyl-2-mercapto-7H-pyrrolo[2,3-d]pyrimidin-4(3H)-one (1.36 g) followed by addition of 1N-sodium hydroxide (7.88 ml) for dissolution. Then, under ice-cooling, a solution of 3-(4-chlorobenzoyl)benzyl bromide (2.79 g) in DME-DMF (6:5; 22 ml) was added dropwise. The mixture was stirred at room temperature for 20 hours, at the end of which time it was poured in ice-water (200ml). The resulting precipitate was collected by filtration and rinsed with water. Then, it was further washed with 50% ethanol/water, methanol and ether in that order, dried, and purified by flash column chromatography (chloroform, containing 1% methanol) to provide the title compound (1.94 g). 1H-NMR (DMSO-d6) δ: 2.25(3H,s), 4.50(2H,s), 6.65(1H,s), 7.50(2H,d,J=8.OHz), 7.69(2H,d,J=8.6Hz), 7.51-7.82(4H,m), 11.38(1H,s), 11.95(1H,s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753664
Source datasetuspto-grants-1998_05
ORD IDord-fc33f09dcb254ddc94af59cb3e531b8d
Source noteuspto-grants-1998_05