Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189789Generated: October 31, 2026

1,2-Dichloroethane → Ethyl 3-[4-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H-indazol-1-yl]propanoate

https://huagongshe.com/reaction/2189789

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant3-Chloro-4-(propan-2-yloxy)benzoic acidHCID 22597728—
ReactantHCID 178471831HCID 178471831—
ReactantHCID 178471848HCID 178471848—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductEthyl 3-[4-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H-indazol-1-yl]propanoateHCID 5931671065.8%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of ethyl 3-{4-[(hydroxyamino)(imino)methyl]-2H-indazol-2-yl}propanoate & ethyl 3-{4-[(hydroxyamino)(imino)methyl]-1H-indazol-1-yl}propanoate (D55) (700 mg, 1.27 mmol) (a 3:1 mix of 1 and 2-isomers), 3-chloro-4-[(1-methylethyl)oxy]benzoic acid (D3) (0.544 g, 2.53 mmol), EDC (0.534 g, 2.79 mmol) and HOBT (0.427 g, 2.79 mmol) in N,N-dimethylformamide (10 ml) was heated at 120° C. for 2 hrs, cooled, diluted with ethyl acetate (60 ml) and washed with water (3×20 ml). The organic layer was dried (MgSO4), evaporated and purified by flash chromatography eluting with EtOAc/hexane 1:4 to give the title compound (380 mg) as a white solid. δH (CDCl3, 400 MHz): 1.17 (3H, t), 1.46 (6H, d), 3.02 (2H, t), 4.10 (2H, q), 4.70-4.77 (3H, m), 7.08 (1H, d), 7.53 (1H, dd), 7.69 (1H, d), 8.05-8.12 (2H, m), 8.29 (1H, d), 8.71 (1H, d). MS (ES): C23H2335ClN4O4 requires 454; found (MH+) 455.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324254B2
Source datasetuspto-grants-2012_12
ORD IDord-5541b79475924df890a966435eec43a6
Source noteuspto-grants-2012_12