Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902489Generated: October 30, 2026

3-Fluorobenzyl bromide → HCID 59702052, compound

https://huagongshe.com/reaction/902489

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluorobenzyl bromideHCID 68007—
ReactantHCID 58727588HCID 58727588—
ReactantHCID 59702060HCID 59702060—
ProductHCID 59702052HCID 59702052—

Reaction Steps

This compound was prepared from 7-[4-(furan-2-carbonyl)-piperazin-1-yl]-5-oxo-4,5-dihydro-thieno[3,2-b]pyridine-6-carboxylic acid ethyl ester (10) and 3-fluoro benzyl bromide by applying a similar method as described for 4-(4-fluoro-benzyl)-7-[4-(furan-2-carbonyl)-piperazin-1-yl]-5-oxo-4,5-dihydro-thieno[3,2-b]pyridine-6-carboxylic acid ethyl ester (11). Yield 210 mg, (22%). 1H-NMR (DMSO-d6): δ 1.28 (t, J=7.2 Hz, 3H), 3.82 (m, 4H), 4.26 (q, J=7.2 Hz, 2H), 5.38 (s, 2H), 6.65 (m, 1H), 7.07 (m, 4H), 7.34 (d, J=5.6 Hz, 1H), 7.37 (m, 1H), 7.88 (m, 1H), 8.03 (d, J=5.6 Hz, 1H); EIMS m/z 510 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365200B2
Source datasetuspto-grants-2008_04
ORD IDord-e654715fc25743bcabb265d849705e1c
Source noteuspto-grants-2008_04