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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261352Generated: November 1, 2026

1-Boc-3-aminopyrrolidine → tert-Butyl 3-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridine-2-carboxamido)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/1261352

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Boc-3-aminopyrrolidineHCID 2756370—
Reactant7-(2-Fluoro-4-nitrophenoxy)thieno[3,2-b]pyridine-2-carbonyl chlorideHCID 59424526—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 3-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridine-2-carboxamido)pyrrolidine-1-carboxylateHCID 5942463720%

Reaction Steps

A solution of 40 (shown in the scheme 7, 600 mg, 1.54 mmol), tert-butyl 3-aminopyrrolidine-1-carboxylate (369 mg, 2.0 mmol) in DCM (15 mL) was stirred overnight at room temperature. The solvent was removed under reduced pressure and the residue was purified by flash column chromatography, eluents EtOAc and EtOAc/MeOH (10:1), to afford the title compound 289 (160 mg, 20%) as an off-white solid. MS (m/z): 503.3 (M+H) (found).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470850B2
Source datasetuspto-grants-2013_06
ORD IDord-95e3768e830a45efb4979f522a535266
Source noteuspto-grants-2013_06