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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1969589Generated: November 2, 2026

(S)-2-(1-(tert-butoxycarbonyl)pyrrolidin-3-yl)acetic acid → HCID 58557467, compound

https://huagongshe.com/reaction/1969589

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-2-(1-(tert-butoxycarbonyl)pyrrolidin-3-yl)acetic acidHCID 1502098—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant2-Hydrazinyl-5-tosyl-5H-pyrrolo[2,3-b]pyrazineHCID 58009810—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 58557467HCID 58557467111.9%

Reaction Steps

To a solution of (S)-3-carboxymethyl-pyrrolidine-1-carboxylic acid tert-butyl ester (0.756 g, 3.30 mmol, AstaTech) and 2-hydrazinyl-5-tosyl-5H-pyrrolo[2,3-b]pyrazine (1.0 g, 3.3 mmol, Example #1, Step D) in DMF (33 mL) was added TEA (1.38 mL, 9.89 mmol) followed by the addition of HATU (1.25 g, 3.30 mmol). The resulting mixture was stirred at ambient temperature for about 15 h then concd under reduced pressure. The residue was taken up in EtOAc (100 mL) and washed with water (100 mL). The organic portion was separated, washed with brine (100 mL), dried over anhydrous Na2SO4, filtered, and concd under reduced pressure to give (S)-tert-butyl 3-(2-oxo-2-(2-(5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)hydrazinyl)ethyl)pyrrolidine-1-carboxylate as a sticky brown solid (1.90 g, 100%). This material was used without further purification: LC/MS (Table 1, Method c) Rt=1.38 min; MS m/z: 515 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426411B2
Source datasetuspto-grants-2013_04
ORD IDord-67523f668e80434897f830a20aa5fe94
Source noteuspto-grants-2013_04