Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187291Generated: November 1, 2026

Methanol → HCID 178501975, compound

https://huagongshe.com/reaction/1187291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium HydroxideHCID 14797—
ReactantBenzyl (2,4-difluoro-3-formylphenyl)carbamateHCID 58086235—
ReactantHCID 178518057HCID 178518057—
SolventHydrochloric AcidHCID 313—
ProductHCID 178501975HCID 17850197592.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

In a reaction vessel, 7H-pyrrolo[2,3-d]pyrimidin-4-ol (37, 855 mg, 6.33 mmol) is combined with (2,4-difluoro-3-formyl-phenyl)-carbamic acid benzyl ester (33, 2.03 g, 6.96 mmol) and potassium hydroxide (1.06 g, 19.0 mmol) and 5 mL of methanol is added. The resulting solution is stirred at 50° C. for 2 days. The reaction is diluted with 1N hydrochloric acid and extracted with ethyl acetate, and the resulting solids collected by filtration and dried under vacuum. The organic layer is separated from the filtrate and the aqueous layer extracted twice more with ethyl acetate. The organic layers are combined and washed with water, brine, dried with magnesium sulfate and filtered. The filtrate is concentrated under vacuum and the resulting material is suspended in acetonitrile and sonicated for 1 hour. The solid is collected by filtration and dried under vacuum, then combined with the first solid collected to provide the desired compound (38, 2.05 g). MS (ESI) [M−H+]−=349.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673928B2
Source datasetuspto-grants-2014_03
ORD IDord-a3fbbaf8030240ccb7f29450e43a7a0b
Source noteuspto-grants-2014_03