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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381718Generated: November 2, 2026

4-Aminobenzoic Acid → HCID 57990405, compound

https://huagongshe.com/reaction/2381718

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminobenzoic AcidHCID 978—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant2-chloro-N-cyclopropyl-5-(pyridin-4-yl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amineHCID 57990302—
Solvent1-ButanolHCID 263—
ProductHCID 57990405HCID 57990405122.2%

Reaction Conditions

Temperature135 °C

Reaction Steps

A mixture of 2-chloro-N-cyclopropyl-5-(pyridin-4-yl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine (245 mg, 0.557 mmol), 4-aminobenzoic acid (150 mg, 1.09 mmol) and trimethylsilyl chloride (0.300 mL, 2.37 mmol) in nBuOH (4 mL) was stirred at 135° C. for 24 h. It was concentrated in vacuo. The residue was purified by HPLC to give butyl 4-(4-amino-5-(pyridin-4-yl)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)benzoate (137 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258144B2
Source datasetuspto-grants-2012_09
ORD IDord-4adc1cf96ce841758a5ab47bf8894d54
Source noteuspto-grants-2012_09