Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348493Generated: October 30, 2026

Ethyl Thioglycolate → [4-(2-tert-Butoxycarbonylaminoethylamino)-5-(4-fluorophenylcarbamoyl)pyrimidin-2-ylsulfanyl]acetic acid ethyl ester

https://huagongshe.com/reaction/348493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl ThioglycolateHCID 12185—
ReactantDiisopropylethylamineHCID 81531—
Reactant{2-[5-(4-Fluorophenylcarbamoyl)-2-methylsulfonyl-pyrimidin-4-ylamino]-ethyl}carbamic acid tert-butyl esterHCID 69523394—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product[4-(2-tert-Butoxycarbonylaminoethylamino)-5-(4-fluorophenylcarbamoyl)pyrimidin-2-ylsulfanyl]acetic acid ethyl esterHCID 6952220558.3%

Reaction Steps

Ethyl thioglycolate (73 μL, 0.66 mmol) was added to a solution of {2-[5-(4-fluorophenylcarbamoyl)-2-methylsulfonyl-pyrimidin-4-ylamino]-ethyl}carbamic acid tert-butyl ester (0.30 g, 0.66 mmol) and DIPEA (117 μL, 0.66 mmol) in DMF (1.5 mL). The resulting solution was stirred under N2 overnight. The reaction mixture was then diluted with ethyl acetate (20 mL) and washed with water (10 mL), 1 N HCl (3×10 mL), water (10 mL), saturated NaHCO3 (3×10 mL), water (10 mL), saturated NaCl (20 mL) and dried over MgSO4. Following filtration, the solvent was removed by rotary evaporation to yield the titled product (0.19 g, 58%) as an off-white solid. 1H NMR: (d6-DMSO) δ 10.25 (s, 1H), 8.63 (m, 1H), 8.57 (s, 1H), 7.65 (m, 2H), 7.16 (m, 2H), 6.91 (t, 1H), 4.08 (q, 2H), 3.96 (s, 2H), 3.44 (m, 2H), 3.08 (m, 2H), 1.31 (s, 9H), 1.16 (t, 3H); HPLC: Rt=4.41 min; MS (ESI): m/z 492.44 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176310B1
Source datasetuspto-grants-2007_02
ORD IDord-1cd39bd4c5b0417fbe6b9b2cc0554672
Source noteuspto-grants-2007_02