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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244705Generated: October 30, 2026

Methoxyacetic Acid → HCID 10288136, compound

https://huagongshe.com/reaction/1244705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethoxyacetic AcidHCID 12251—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 11772963HCID 11772963—
SolventDichloromethaneHCID 6344—
ProductHCID 10288136HCID 1028813620.1%

Reaction Steps

DIPEA (180 μL, 1.05 mmol), HOBT (68 mg, 0.5 mmol), methoxyacetic acid (0.5 mmol, 38 μL) and EDAC (120 mg, 0.63 mmol) were added to a suspension of N-[(1R,2R)-1-amino-2,3-dihydro-1H-inden-2-yl]-2,3-dichloro-4H-thieno[3,2-b]pyrrole-5-carboxamide (Method 8, 240 mg, 0.5 mmol) in anhydrous DCM (7 mL). The reaction was stirred at ambient temperature for approximately 16 h. The volatiles were removed by evaporation under reduced pressure, the residue dissolved in EtOAc (10 mL), washed with water (2×10 mL), brine (10 mL) and dried (MgSO4). The volatiles were removed by evaporation under reduced pressure and the residue was purified by flash column chromatography on SiO2 (1:1 EtOAc:isohexane); the solvent removed by evaporation under reduced presssure and dried to give the title compound (44 mg, 20%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122567B2
Source datasetuspto-grants-2006_10
ORD IDord-af1586ed370e473899d53a1d21fc42c6
Source noteuspto-grants-2006_10