Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646772Generated: October 31, 2026

Diisopropylethylamine → 1,1-Dimethylethyl (3S)-3-[[(3-amino-6-bromo-2-pyrazinyl)carbonyl]amino]-1-piperidinecarboxylate

https://huagongshe.com/reaction/646772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-butyl (3S)-3-aminopiperidine-1-carboxylateHCID 1501975—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant3-Amino-6-bromopyrazine-2-carboxylic acidHCID 18521600—
SolventWaterHCID 962—
Product1,1-Dimethylethyl (3S)-3-[[(3-amino-6-bromo-2-pyrazinyl)carbonyl]amino]-1-piperidinecarboxylateHCID 5871058975%

Reaction Steps

3-amino-6-bromopyrazine-2-carboxylic acid (3.63 g, 16.65 mmol), HATU (9.49 g, 25.0 mg) and DIEA (4.35 mL, 25.0 mmol) was added to a solution of (s)-3-amino-piperidine-1-carboxylic acid tert-butyl ester (4.00 g, 19.97 mmol, commercially available from Astatech or Arch Corporation). It was stirred at room temperature overnight. The reaction mixture was poured into water (200 mL), and extracted with ethyl acetate (2×150 mL) then dried over anhydrous sodium sulfate and filteration, concentration and purified by column chromatography to give 1,1-dimethylethyl (3S)-3-{[(3-amino-6-bromopyrazin-2-yl)carbonyl]amino}piperidine-1-carboxylate 5.00 g (75.0% yield): MS (EI) for C15H22BrN5O3: 401.12 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07704995B2
Source datasetuspto-grants-2010_04
ORD IDord-39cdc3000770407ea2ca8f5d1c6c20cd
Source noteuspto-grants-2010_04