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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670644Generated: October 31, 2026

Pyridine → HCID 178512083, compound

https://huagongshe.com/reaction/1670644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTriethylamineHCID 8471—
ReactantDiphenyl N-CyanocarbonimidateHCID 688090—
ReactantHCID 57748742HCID 57748742—
CatalystPlatinumHCID 23939—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178512083HCID 17851208340.2%

Reaction Steps

Dissolve [4-((E)-3,7-difluoro-6H-dibenzo[b,e]oxepin-11-ylidenemethyl)-2-nitro-phenyl]-((7S,8aS)-hexahydro-pyrrolo[2,1-c][1,4]oxazin-7-yl)-amine (0.009 mol, 5.0 g) in tetrahydrofuran (40 mL). Add triethylamine (0.009 mol, 0.9 g) and 10% platinum on carbon (1.0 g) and hydrogenate in a Parr shaker at 50 psi (H2) at room temperature for 3 h. Filter off the catalyst through a plug of diatomaceous earth, add pyridine (40 mL) and diphenyl N-cyanocarbonimidate (0.009 mol, 2.35 g) to the filtrate. Stir at room temperature for 16 h, then heat at 60-70° C. for 8 h. Remove the solvent under reduced pressure. Dissolve the resulting residue in dichloromethane and wash with water and saturated sodium bicarbonate solution. Dry the organic layer over anhydrous sodium sulfate, filter, and concentrate under reduced pressure. Purify on a silica gel column using 1% methanol in dichloromethane as eluent to give the title compound (1.9 g, 36%). LC-MS m/z 526.4 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994164B2
Source datasetuspto-grants-2011_08
ORD IDord-4497e23b06134d84963570bd684f54d9
Source noteuspto-grants-2011_08