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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582541Generated: October 30, 2026

2-Aminophenol → HCID 70345659, compound

https://huagongshe.com/reaction/582541

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminophenolHCID 5801—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 86647542HCID 86647542—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 70345659HCID 703456598%

Reaction Steps

A mixture of 1-[2-chloro6-[(2,2-diphenylethyl)amino]-9H-purin-9-yl]-1-deoxy-N-ethyl-β-D-ribofuranuronamide (0.20 g, 0.38 mmol), 2-aminophenol (0.20 g, 1.83 mmol), 1,8-diazabicyclo[5.4.0]undec-7-ene (0.052 ml, DBU) and dimethylsulphoxide (1 ml) was stirred and heated at 140° C. under nitrogen for 6h, and then left at 21° C. overnight. The mixture was partitioned between ethyl acetate (200 ml) and water (40 ml). The aqueous layer was extracted with more ethyl acetate (50 ml) and the total organic solution was washed (water, 20 ml), dried (Na2SO4) and evaporated. The residue was purified on flash silica eluting with dichloromethane:methanol (19:1), and then by preparative TLC (20×20 cm plate with 2 mm layer of Kieselgel 60 F254 ; Art 5717) in dichloromethane:ethyl acetate:ethanol 9:9:2, and then by preparative HPLC (30 to 70% acetonitrile) to give the title compound (0.018 g) as a cream foam, MH+ =596. Analysis found: C,52.2, H,4.3, N,11.8; C32H33N7O5.2CF3CO2H requires C,52.5, H,4.3, N,11.9%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05925624
Source datasetuspto-grants-1999_07
ORD IDord-8368726679094119a5442ba3b66b0e29
Source noteuspto-grants-1999_07