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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504333Generated: October 31, 2026

Diisopropylethylamine → HCID 86682809, compound

https://huagongshe.com/reaction/1504333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 67495583HCID 67495583—
ReactantHCID 76848194HCID 76848194—
SolventDimethylformamideHCID 6228—
ProductHCID 86682809HCID 8668280971%

Reaction Steps

To a solution of 4-bromo-2-fluoro-3-(trifluoromethoxy)benzoic acid (150 mg, 0.50 mmol, Preparation 52), (R)-tert-butyl 4-(5-aminopyridin-2-yl)-3-methylpiperazine-1-carboxylate (145 mg, 0.50 mmol), and HATU (235 mg, 0.62 mmol) dissolved in DMF (1 mL) was added DIPEA (0.43 mL, 2.48 mmol). The reaction mixture was stirred at RT for 1 h, extracted with EtOAc (80 mL) washed with water (3×20 mL) and brine (20 mL), dried over sodium sulfate, filtered, concentrated, and purified by silica gel chromatography (12 g silica gel, 0-40% EtOAc:hexanes over 20 min), to provide the title intermediate (203 mg, 71% yield) as a yellow solid. (m/z): [M+H]+ calcd for C23H25BrF4N4O4 577.10; 579.10. found 579.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212168B2
Source datasetuspto-grants-2015_12
ORD IDord-86a28017ff154d9eb6e7ccd913677095
Source noteuspto-grants-2015_12