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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 907172Generated: October 31, 2026

Bromoacetic Acid → HCID 59430591, compound

https://huagongshe.com/reaction/907172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetic AcidHCID 6227—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 59425699HCID 59425699—
SolventAcetonitrileHCID 6342—
ProductHCID 59430591HCID 5943059164.7%

Reaction Steps

Bromoacetic acid (52 mg, 0.37 mmol) was combined with EDCI hydrochloride (62 mg, 0.4 mmol) and acetonitrile (900 μL) to form a homogeneous solution. 2-(3-Amino-4-hydroxyphenyl)-1-ethyl-6-methoxy-1H-indole-3-carbonitrile (100 mg, 0.33 mmol), prepared as in example 1BG, step B, was added to the solution. A thick paste soon formed. Another 1.1 mL of acetonitrile was added and the mixture was then stirred at room temperature for 2 hours. The reaction mixture was then partitioned between H2O and EtOAc. The organic layer was dried and concentrated. Purification by silica gel chromatography (4/1, CH2Cl2/EtOAc) yielded 2-chloro-N-[5-(3-cyano-1-ethyl-6-methoxy-1H-indol-2-yl)-2-hydroxyphenyl] acetamide (82 mg, 60%), compound 333, as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08013006B2
Source datasetuspto-grants-2011_09
ORD IDord-41395d7358734ce0b12940f479f7e261
Source noteuspto-grants-2011_09