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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416217Generated: October 27, 2026

Diisopropylethylamine → Methyl 4-[(4-thiophen-3-yl-pyrimidin-2-ylamino)-methyl]-benzoate

https://huagongshe.com/reaction/416217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 4-(aminomethyl)benzoateHCID 571728—
Reactant2-Chloro-4-(thiophen-3-yl)pyrimidineHCID 14117942—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 4-[(4-thiophen-3-yl-pyrimidin-2-ylamino)-methyl]-benzoateHCID 5893056948%

Reaction Conditions

Temperature130 °C

Reaction Steps

To a solution of 14 (680 mg, 3.46 mmol) and methyl 4-(aminomethyl)benzoate (686 mg, 4.51 mmol) in dry 1,4-dioxane (10 mL) was added DIPEA (1.50 mL, 8.65 mmol) and the mixture was heated for 48 h at 130° C. in a sealed tube. Solvents were removed under vacuum and the residue was triturated with a mixture of EtOAc/Et2O, to form a solid, which was collected by filtration and dried. This material was purified by flash chromatography on silica gel (EtOAc/CH2Cl2: 30/70) to afford the title compound 15 (540 mg, 1.66 mmol, 48% yield). 1H NMR: (400 MHz, DMSO-d6) δ (ppm): 8.29-8.23 (m, 2H), 7.88 (d, J=8.4 Hz, 2H), 7.84-7.77 (m, 1H), 7.69-7.59 (m, 2H), 7.52-7.43 (m, 2H), 7.03 (d, J=5.2 Hz, 1H), 4.60 (d, J=6.4 Hz, 2H), 3.81 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088805B2
Source datasetuspto-grants-2012_01
ORD IDord-5de42867bb1e4e91b88b7035e774ccd8
Source noteuspto-grants-2012_01