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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506063Generated: November 3, 2026

Hydrochloric Acid → HCID 59425830, compound

https://huagongshe.com/reaction/506063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 59425665HCID 59425665—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 59425830HCID 5942583078%

Reaction Steps

2-[4-(2-Azidoethoxy)phenyl]-1-ethyl-6-methoxy-1H-indole-3-carbonitrile (410 mg, 1.14 mmol), prepared as in step A, above, is suspended in a solution of MeOH (20 mL) and concentrated HCl (500 μL). Pd/C (150 mg, 10%) is added, and this mixture is hydrogenated at 30 p.s.i. for 1 h. This is filtered and the filtrate is concentrated. The filtrate residue is partitioned between EtOAc and 0.5N NaOH. The organic layer is dried and concentrated. Purification by silica gel chromatography (10-30%, MeOH/CH2Cl2) yields 2-[4-(2-aminoethoxy)phenyl]-1-ethyl-6-methoxy-1H-indole-3-carbonitrile (298 mg, 78%), compound 267, as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781478B2
Source datasetuspto-grants-2010_08
ORD IDord-de87b7f41ee041f184eae3ea3f5bb6a6
Source noteuspto-grants-2010_08