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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2365777Generated: November 4, 2026

Formic Acid → HCID 45380997, compound

https://huagongshe.com/reaction/2365777

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantHydrochloric AcidHCID 313—
Reactant3-(Trifluoromethyl)phenyl isocyanateHCID 9483—
ReactantHCID 58506754HCID 58506754—
SolventDichloromethaneHCID 6344—
ProductHCID 45380997HCID 45380997—

Reaction Steps

A solution of (R)-tert-butyl 3-(4-amino-3-(4-aminophenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)pyrrolidine-1-carboxylate (0.090 g, 0.23 mmol) in CH2Cl2 (10 mL) was cooled in an ice-water bath. To this, 3-(trifluoromethyl)phenyl isocyanate (0.032 mL, 0.23 mmol) diluted in CH2Cl2 (5 mL) was added dropwise. The reaction was allowed to warm to room temperature and left stirring for 6 hours. After, formic acid (5 mL) and concentrated HCl (0.5 mL) were added dropwise directly to the reaction mixture. Three major species were observed by LC-MS corresponding to AD73a, AD73b, and AD73c. The reaction mixture was left stirring for 12 hours and then was concentrated in vacuo, resuspended in 50:50 H2O—CH3CN, and purified on a C18 column in CH3CN/H2O/0.1% TFA (1-100% gradient) to afford AD73a (ESI-MS m/z [M+H]+ found 483.5, calculated 483.2), AD73b (ESI-MS m/z [M+H]+ found 483.5, calculated 483.2), and AD73c (ESI-MS m/z [M+H]+ found 670.5, calculated 670.2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697709B2
Source datasetuspto-grants-2014_04
ORD IDord-b3c48045e03e4216a6f586275ffea493
Source noteuspto-grants-2014_04