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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478903Generated: November 4, 2026

N-bromobutanimide → HCID 67353647, compound

https://huagongshe.com/reaction/1478903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 67354512HCID 67354512—
SolventDichloromethaneHCID 6344—
ProductHCID 67353647HCID 6735364798%

Reaction Steps

To an ice-cooled solution of methyl 1-ethyl-1H-pyrrolo[3,2-c]pyridine-6-carboxylate (IF, 700 mg, 3.43 mmol) in DCM (5 ml) was added NBS (610 mg, 3.43 mmol). The reaction mixture was stirred at room temperature for 10 min. The reaction mixture was concentrated in vacuo and purified by chromatography (SiO2, EtOAc) to give methyl 3-bromo-1-ethyl-1H-pyrrolo[3,2-c]pyridine-6-carboxylate (3A, 950 mg, 3.36 mmol, 98% yield) as a white powder. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.52 (t, J=7.33 Hz, 3 H) 4.04 (s, 3 H) 4.25 (q, J=7.33 Hz, 2 H) 7.33 (s, 1 H) 8.22 (d, J=0.76 Hz, 1 H) 8.92 (d, J=1.01 Hz, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403819B2
Source datasetuspto-grants-2016_08
ORD IDord-3e9efdeaf122484fae22845a2d1769c4
Source noteuspto-grants-2016_08