Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878707Generated: November 1, 2026

Sodium hydride → HCID 59843078, compound

https://huagongshe.com/reaction/1878707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant5-Bromo-2-hydroxypyridineHCID 599528—
Reactanttert-Butyl N-(2-bromoethyl)carbamateHCID 4103526—
SolventDimethylformamideHCID 6228—
ProductHCID 59843078HCID 59843078—

Reaction Conditions

Temperature23 °C

Reaction Steps

To a stirring solution of 5-bromo-2(1h)-pyridone (550 mg, 3161 μmol) in DMF (5 mL) under nitrogen was added NaH (60% dispersion in mineral oil; 152 mg, 6322 μmol). After for 10 min, 2-(boc-amino) ethyl bromide (779 mg, 3477 μmol) was added. The mixture was stirred for 18 h at 23° C. The mixture was partitioned between CH2Cl2 and 5% NaHCO3. The aqueous was extracted with CH2Cl2 (10 mL) twice. The combined organics were dried over MgSO then concentrated to a solid from toluene under reduced pressure. The residue was purified on silica (40 g) eluting with 0-30% of 5% MeOH/CH2Cl2 to give the product as a white solid. MS (ESI pos. ion) m/z (MH+): 317/319. Calc'd exact mass for C12H17BrN2O3: 316. 1H NMR (400 MHz, Chloroform-d) δ ppm 1.44 (s, 9H) 3.45 (q, J=6.02 Hz, 2H) 4.03-4.09 (m, 2H) 4.92 (br. s., 1H) 6.48 (d, J=10.04 Hz, 1H) 7.34-7.39 (m, 2H). 13C NMR (101 MHz, Chloroform-d) δ ppm 26.08, 37.26, 47.20, 95.56, 119.79, 135.87, 140.53

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314087B2
Source datasetuspto-grants-2012_11
ORD IDord-2d0ccf521f484c689c11a626009de591
Source noteuspto-grants-2012_11