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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207062Generated: November 2, 2026

2-Mesitylenesulfonyl chloride → 2-Amino-5-(4-(hydroxymethyl)-2-methoxybenzyl)-6-methylpyrimidin-4-yl 2,4,6-trimethylbenzenesulfonate

https://huagongshe.com/reaction/2207062

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Mesitylenesulfonyl chlorideHCID 13046—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178492557HCID 178492557—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Amino-5-(4-(hydroxymethyl)-2-methoxybenzyl)-6-methylpyrimidin-4-yl 2,4,6-trimethylbenzenesulfonateHCID 8794515184.8%

Reaction Steps

2-Mesitylenesulfonyl chloride (7.2 g) was added to a suspension of diisopropylethylamine (5.5 mL) and the product from step (iii) (6.1 g) in THF (200 mL) and the mixture was stirred under reflux for 12 h. The resulting mixture was diluted with water and extracted with EtOAc. The combined organic layer was washed with brine, dried and concentrated under reduced pressure. The residue was purified by flash column chromatography on amino silica gel to afford the sub-title compound (8.6 g) as a white solid; 1H NMR (300 MHz, CDCl3); 6.92 (2H, s), 6.86 (1H, s), 6.77 (2H, s), 4.67 (2H, br s), 4.64 (2H, d), 3.82 (3H, s), 3.81 (2H, s), 2.57 (6H, s), 2.29 (3H, s), 2.21 (3H, s), 1.81 (1H, t).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376398B2
Source datasetuspto-grants-2016_06
ORD IDord-df674a0063ca4e19ad7a93671e2187e2
Source noteuspto-grants-2016_06