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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351895Generated: November 2, 2026

HCID 57140123, compound → HCID 18007376, compound

https://huagongshe.com/reaction/1351895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57140123HCID 57140123—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventChlorobenzeneHCID 7964—
ProductHCID 18007376HCID 18007376124.8%

Reaction Steps

A mixture of (2S)-1-[N-benzyl-N-(2-chloro-3-methoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-yl)amino]-3-phenoxy-2-propanol (172 mg) and 10% palladium on activated carbon (50% wet, 50 mg) in a mixture of chlorobenzene (2 ml) and methanol (2 ml) was stirred at room temperature in the presence of hydrogen at an atmospheric pressure for 2 hours. After filtration, the filtrate was evaporated in vacuo. The residue was purified by column chromatography on silica gel (chloroform:methanol=20:1 to 10:1) and followed by treatment with 4N hydrogen chloride in ethyl acetate to give 1-(2-chloro-3-methoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-yl)amino-3-phenoxy-2-propanol hydrochloride (95 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217706B2
Source datasetuspto-grants-2007_05
ORD IDord-f995522e7d1144909f253a2ae44d5496
Source noteuspto-grants-2007_05