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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174840Generated: October 31, 2026

Sodium Iodide → 3-[3-(5-Amino-3-tert-butyl-pyrazol-1-yl)-phenoxy]-propan-1-ol

https://huagongshe.com/reaction/1174840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Chloro-1-propanolHCID 12313—
Reactant3-(5-amino-3-tert-butyl-1H-pyrazol-1-yl)phenolHCID 59557966—
Solvent1-ButanolHCID 263—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product3-[3-(5-Amino-3-tert-butyl-pyrazol-1-yl)-phenoxy]-propan-1-olHCID 5955795480%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 3-(5-amino-3-tert-butyl-pyrazol-1-yl)-phenol (400 mg, 1.73 mmol), 3-chloropropanol (326 mg, 3.46 mmol), potassium carbonate (596 mg, 4.32 mmol) and sodium iodide (77 mg, 0.52 mmol) were combined in n-butanol (6 mL). The reaction mixture was heated at 60° C. for 4 days. The mixture was cooled to room temperature, water (100 mL) and EtOAc (100 mL) were added, and then the organic phase was washed with water and brine, dried (Na2SO4), and concentrated at reduced pressure. The residue was purified by MPLC (80:20 hexane/EtOAc) to give the product 3-[3-(5-amino-3-tert-butyl-pyrazol-1-yl)-phenoxy]-propan-1-ol (400 mg, 80%). 1H-NMR (DMSO-d6) δ 7.30 (t, 1H), 7.10 (m, 2H), 6.80 (d, 1H), 5.30 (s, 1H), 5.10 (bs, 2H), 4.0 (t, 2H), 3.60 (t, 3H), 1.80 (m, 2H), 1.30 (s, 9H); MS LC-MS [M+H]+=290.3, RT=1.05 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838524B2
Source datasetuspto-grants-2010_11
ORD IDord-65dd54a01c764275ab072d5cd7b9019c
Source noteuspto-grants-2010_11