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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930405Generated: October 31, 2026

Ethyl 4-(Isopropylamino)-2-(methylthio)pyrimidine-5-carboxylate → (4-(Isopropylamino)-2-(methylthio)pyrimidin-5-yl)methanol

https://huagongshe.com/reaction/1930405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-(Isopropylamino)-2-(methylthio)pyrimidine-5-carboxylateHCID 10491237—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(4-(Isopropylamino)-2-(methylthio)pyrimidin-5-yl)methanolHCID 1053655298.4%

Reaction Steps

To a solution of ethyl 4-(isopropylamino)-2-(methylthio)pyrimidine-5-carboxylate (16.4 g, 64.4 mmol) in anhydrous THF (100 mL) was added LAH (6.1 g, 0.16 mol) in portions at 0° C. under N2 atmosphere, then the reaction mixture was stirred at r.t. for 30 min. The reaction was quenched by the addition of water (6 mL) followed by aqueous solution of 2N NaOH (6 mL). The suspension was filtered and the filtrate was concentrated to give (4-(isopropylamino)-2-(methylthio)pyrimidin-5-yl)methanol (13.5 g, 98.4% yield), which was used in next step without further purification. 1HNMR (400 MHz, DMSO-d6): δ 7.79 (s, 1 H), 6.37 (d, J=7.6 Hz, 1 H), 5.10 (t, J=5.6 Hz, 1 H), 4.28-4.20 (m, 3 H), 2.38 (s, 3 H), 1.13 (d, J=6.4 Hz, 6 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188113B2
Source datasetuspto-grants-2012_05
ORD IDord-d25903d80d4744eabcea82687f40558a
Source noteuspto-grants-2012_05