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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912778Generated: November 1, 2026

HCID 178418361, compound → HCID 23155176, compound

https://huagongshe.com/reaction/1912778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178513227HCID 178513227—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductHCID 23155176HCID 2315517627.4%

Reaction Steps

In 10 mL of methanol, 12 mg (0.025 mmol) of 1-{4-[3-(4-chloro-3-(trifluoromethyl)phenyl)ureido]phenyl}-N-hydroxy-1H-indole-5-carboxamidine was dissolved and the solution was subjected to hydrogenation catalytic reduction on 10% palladium carbon in a hydrogen atmosphere at room temperature for 14 hours. After removal of the palladium carbon by a membrane filter, the filtrate was concentrated under reduced pressure, and the obtained product was triturated from diethyl ether to obtain 3 mg (25%) of 1-{4-[3-(3-(trifluoromethyl)phenyl)-ureido]phenyl}-1H-indole-5-carboxamidine (Table 1, Compound No. 25).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609656B2
Source datasetuspto-grants-2013_12
ORD IDord-fc634fdba292458b89c5455265eeafd7
Source noteuspto-grants-2013_12