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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091552Generated: November 2, 2026

Allyl Alcohol → HCID 59286706, compound

https://huagongshe.com/reaction/1091552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl AlcoholHCID 7858—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 24958894HCID 24958894—
SolventDimethylformamideHCID 6228—
ProductHCID 59286706HCID 5928670677.3%

Reaction Conditions

Temperature42.5 °C

Reaction Steps

(R)-5-cyclopentyl-6-ethyl-3-(2-methoxy-4-(methylcarbamoyl)phenylamino)-5,6-dihydroimidazo[1,5-f]pteridine-7-carboxylic acid 1-2 (44 mg, 0.09 mmol) in DMF (0.5 mL) was treated with carbonyldiimidazole (19 mg, 0.12 mmol) and stirred at 40-45° C. for 40 minutes. Allyl alcohol (1 ml, 14.7 mmol) was then added and the reaction mixture was stirred at 40° C. for 18 hours. The mixture was partitioned between an aqueous solution of sodium carbonate and ethyl acetate. The organic phase was washed with brine, dried over magnesium sulphate and concentrated to give the desired compound as a pale brown solid (37 mg, 77% yield); LC/MS M+1 (obs.) 532.68, LC/MS M-1 (obs.) 530.81.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129387B2
Source datasetuspto-grants-2012_03
ORD IDord-bf17e9e84e684b0fb37c181159656608
Source noteuspto-grants-2012_03