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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169734Generated: October 30, 2026

Sodium Carbonate → 3-(2-Chloro-5-(2-thienyl)pyrimidine-4-ylamino)propanol

https://huagongshe.com/reaction/1169734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTris(furan-2-yl)phosphaneHCID 521585—
Reactant2-Thiopheneboronic acidHCID 2733960—
Reactant3-(2-Chloro-5-iodopyrimidine-4-ylamino)propan-1-olHCID 59550848—
Solvent1,2-DimethoxyethaneHCID 8071—
Product3-(2-Chloro-5-(2-thienyl)pyrimidine-4-ylamino)propanolHCID 58985646—

Reaction Conditions

Temperature75 °C

Reaction Steps

In accordance with procedure 3, 3-(2-chloro-5-iodopyrimidine-4-ylamino)propan-1-ol (1.38 g, 4.4 mmol) and 2-thiophenboronic acid (0.62 g, 4.87 mmol) are dissolved in 15 ml dimethoxyethane under argon, and tri(2-furyl)phosphine (104 mg, 0.45 mmol) and 1 molar Na2CO3 soln. (7.1 ml, 7.1 mmol) are added (the previously light yellow reaction mixture becomes almost colourless and turbid after the Na2CO3 addition). Argon is passed in for 15 mins. Tetrakis(triphenyl-phosphine)palladium (511 mg, 0.44 mmol) is then added and the reaction mixture is stirred for 18 hrs at 75° C. under argon (suspension). Dimethoxyethane is distilled off on the rotary evaporator, the residue treated with 250 ml ethyl acetate and 30 ml H2O, stirred vigorously for 30 mins, and the undissolved substance filtered off at the pump on a G4 frit, and washed with H2O and ethyl acetate: 372 mg residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825128B2
Source datasetuspto-grants-2010_11
ORD IDord-6cbfa82787ca4bb193e27087cc1e8176
Source noteuspto-grants-2010_11