Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821597Generated: November 1, 2026

Triethylamine → HCID 69060367, compound

https://huagongshe.com/reaction/1821597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantBoc-L-ValineHCID 83693—
ReactantIsopropenyl chloroformateHCID 93846—
ReactantHCID 16117146HCID 16117146—
SolventDichloromethaneHCID 6344—
ProductHCID 69060367HCID 6906036751.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

[6-(2,4-Difluoro-phenoxy)-3-(2,5-difluoro-phenyl)-4-(2-methanesulfonyl-ethylamino)-pyrazolo[3,4-d]pyrimidin-1-yl]-methanol (170 mg, 0.33 mmol) was dissolved in methylene chloride, and Boc-(L)-Valine (216 mg, 0.99 mmol), dimethylamino pyridine (81 mg, 0.66 mmol), and triethylamine (0.23 mL, 1.6 mmol) were added. The reaction mixture was cooled to 0° C. and stirred under nitrogen, and isopropenyl chloroformate (54 uL, 0.49 mmol) was added. The reaction mixture was stirred for 10 minutes and then partitioned between water and methylene chloride. The organic layer was washed with brine, dried (MgSO4), filtered and concentrated under reduced pressure. The residue was purified by flash chromatography through silica (1:1 hexanes/EtOAc) to give 120 mg of 2-tert-butoxycarbonylamino-3-methyl-butyric acid 6-(2,4-difluoro-phenoxy)-3-(2,5-difluoro-phenyl)-4-(2-methanesulfonyl-ethylamino)-pyrazolo[3,4-d]pyrimidin-1-ylmethyl ester as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608603B2
Source datasetuspto-grants-2009_10
ORD IDord-83307cd99db84c60ab6e5cff4c841983
Source noteuspto-grants-2009_10