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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706345Generated: October 29, 2026

Trifluoroacetic acid → HCID 71555379, compound

https://huagongshe.com/reaction/706345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 89535919HCID 89535919—
SolventDichloromethaneHCID 6344—
ProductHCID 71555379HCID 7155537913.6%

Reaction Steps

To a solution of 27-1 (100 mg, 0.32 mmol) and Boc-glycine (68 mg, 0.39 mmol) in DCM (10 mL) was added TEA (98 mg, 0.96 mmol) and HATU (184 mg, 0.48 mmol). the mixture was stirred at rt for 16 h. The mixture then washed with saturated sodium bicarbonate solution (aq), and the organic layer was dried and evaporated. The residue was purified by column chromatography to yield tert-butyl(2-((3-((3-((1H-pyrrolo[2,3-b]pyridin-4-yl)methyl)thioureido)methyl)phenyl)amino)-2-oxoethyl)carbamate (120 mg, 0.26 mmol). To a solution of tert-butyl(2-((3-((3-((1H-pyrrolo[2,3-b]pyridin-4-yl)methyl)thioureido)methyl)phenyl)amino)-2-oxoethyl)carbamate (120 mg, 0.26 mmol) in DCM (10 mL) was added TFA (2 mL). The mixture was stirred at rt for 0.5 h. Solvent was evaporated and the residue was purified by semi-prep HPLC to yield Example 112, N-(3-((3-((1H-pyrrolo[2,3-b]pyridin-4-yl)methyl)thioureido)methyl)phenyl)-2-aminoacetamide (13 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174984B2
Source datasetuspto-grants-2015_11
ORD IDord-6a70b336546f4853b2ee266526d43242
Source noteuspto-grants-2015_11