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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092856Generated: October 31, 2026

(3S)-(-)-3-(tert-Butoxycarbonylamino)pyrrolidine → HCID 58317729, compound

https://huagongshe.com/reaction/2092856

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3S)-(-)-3-(tert-Butoxycarbonylamino)pyrrolidineHCID 1514396—
Reactant4,6-dichloro-2-[(2,4-dimethoxyphenyl)methyl]-7-fluoro-1H,2H,3H-pyrrolo[3,4-c]pyridin-3-oneHCID 58317575—
SolventAcetonitrileHCID 6342—
ProductHCID 58317729HCID 5831772955.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

A tube containing 4,6-dichloro-2-(2,4-dimethoxybenzyl)-7-fluoro-1H-pyrrolo[3,4-c]pyridin-3(2H)-one (300 mg, 0.808 mmol) and (S)-tert-butyl pyrrolidin-3-ylcarbamate (301 mg, 1.616 mmol) dissolved in ACN (4 mL) was sealed and heated at 100° C. for 2 d. The reaction mixture was concentrated and dissolved in EtOAc (20 mL) and washed with saturated aq NaHCO3 (10 mL) and brine (10 mL). The organic extracts were dried over Na2SO4 and evaporated to give a crude product, which was purified via preparative HPLC. Pure fractions were collected and evaporated to give the title compound (235 mg, 55.8%). [M+H] calc'd for C25H30ClFN4O5, 521. found, 521.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440689B2
Source datasetuspto-grants-2013_05
ORD IDord-e2e4e83c1fa241808c05288cccb35814
Source noteuspto-grants-2013_05