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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006266Generated: November 1, 2026

2-Chlorobenzoxazole → HCID 22676839, compound

https://huagongshe.com/reaction/1006266

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzoxazoleHCID 11986—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 22676742HCID 22676742—
SolventDimethylformamideHCID 6228—
SolventSodium BicarbonateHCID 516892—
ProductHCID 22676839HCID 2267683997%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of Ethyl 1-(3-methoxybenzyl)-3-(4-methoxyphenyl)-5-[2-(methylamino)ethoxy]-1H-indole-2-carboxylate (Example 156, 100 mg, 0.2028 mmol) in N,N-dimethylformamide (1.5 ml) was added diisopropylethylamine (0.09 ml, 0.5167 mmol, 2.5 eq.) and 2-chlorobenzoxazole (0.03 ml, 0.2636 mmol, 1.3 eq.). The reaction mixture was heated at 120° C. for 4 hr. After cooling the reaction was diluted with saturated aqueous sodium bicarbonate and then extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over anhydrous Na2SO4, concentrated in vacuo and purified by flash column (silica gel, dichloromethane to dichloromethane:methanol 95:5). The desired product was obtained as a light yellow oil in 97% yield (119 mg), MS (M+H)=606.3, Rf=0.69 (dichloromethane/methanol 95:5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787651B2
Source datasetuspto-grants-2004_09
ORD IDord-ac418d80c7e14fc2bb1346103850165e
Source noteuspto-grants-2004_09