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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797493Generated: November 2, 2026

Dimethylformamide → HCID 69365248, compound

https://huagongshe.com/reaction/1797493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant1-FluorenemethanolHCID 52307—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantHCID 22176086HCID 22176086—
SolventWaterHCID 962—
ProductHCID 69365248HCID 6936524882.8%

Reaction Steps

A solution of 4-butoxy-3-{{(tert-butoxycarbonyl)amino}methyl}-2-isobutyl-1-oxo-1,2-dihydro-6-isoquinolinecarboxylic acid (synthesized according to the method similar to that in Example 76 (1)) (0.45 g, 1 mmol), diphenylphosphoryl azide (0.26 ml, 1.2 mmol) and triethylamine (0.17 ml, 1.2 mmol) in N,N-dimethylformamide, (10 ml) was stirred at room temperature for 1 h. The reaction mixture was poured into water and extracted with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was dissolved in toluene (20 ml) and the mixture was refluxed with stirring for 1 h. To the obtained mixture was added 9H-fluorenylmethanol (0.29 g, 1.5 mmol) and the mixture was refluxed with stirring for 1 h. The reaction mixture was poured into water and extracted with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography and recrystallized from tetrahydrofuran-diisopropyl ether to give 9H-fluoren-9-ylmethyl 4-butoxy-3-{{(tert-butoxycarbonyl)-amino}methyl}-2-isobutyl-1-oxo-1,2-dihydro-6-isoquinolinylcarbamate (0.53 g, 82.8%) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034039B2
Source datasetuspto-grants-2006_04
ORD IDord-00641ac09ca342e2a0d93ca6f274c5a9
Source noteuspto-grants-2006_04