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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420314Generated: November 3, 2026

2-Aminophenol → HCID 70345659, compound

https://huagongshe.com/reaction/1420314

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 7034565979.5%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 1-[2-chloro-6-[(2,2-diphenylethyl)amino]-9H-purin-9-yl]-1-deoxy-N-ethyl-β-D-ribofuranuronamide (0.20 g, 0.038 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 6 h, 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 numberUS05889178
Source datasetuspto-grants-1999_03
ORD IDord-b6a561c28be54875984f90af75eae747
Source noteuspto-grants-1999_03