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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250440Generated: October 31, 2026

1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-5-(2-methoxy-ethoxy)-1H-pyrrolo[2,3-c]pyridine-2-carboxylic acid ethyl ester → 1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-5-(2-methoxy-ethoxy)-1H-pyrrolo[2,3-c]pyridine-2-carboxylic acid

https://huagongshe.com/reaction/2250440

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-5-(2-methoxy-ethoxy)-1H-pyrrolo[2,3-c]pyridine-2-carboxylic acid ethyl esterHCID 69225100—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-5-(2-methoxy-ethoxy)-1H-pyrrolo[2,3-c]pyridine-2-carboxylic acidHCID 67011223—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 1.3 g (2.814 mmol) 1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-5-(2-methoxy-ethoxy)-1H-pyrrolo[2,3-c]pyridine-2-carboxylic acid ethyl ester in 30 mL THF and 15 mL MeOH 11.26 mL 1M LiOH solution were added and the mixture was stirred at 50° C. for 3 h. The organic solvents were removed in vacuo, 50 mL of water were added and the pH was adjusted to pH 2 with 1N HCl solution. The desired product precipitated and was filtered, washed with water and dried over P2O5. Yield 1.11 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317027B2
Source datasetuspto-grants-2008_01
ORD IDord-19f71d02c8dc44068a3879f400ebd557
Source noteuspto-grants-2008_01