Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297797Generated: October 30, 2026

2-Thiopheneboronic acid → (1H-Indol-5-yl)-(2-thiophen-2-yl-thieno[3,2-b]pyridin-7-yl)-amine

https://huagongshe.com/reaction/2297797

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiopheneboronic acidHCID 2733960—
Reactant(2-bromo-thieno[3,2-b]pyridin-7-yl)-(1H-indol-5-yl)-amineHCID 18382766—
Product(1H-Indol-5-yl)-(2-thiophen-2-yl-thieno[3,2-b]pyridin-7-yl)-amineHCID 9884654—

Reaction Steps

The title compound was prepared from thiophene-2-boronic acid and (2-bromo-thieno[3,2-b]pyridin-7-yl)-(1H-indol-5-yl)-amine by a procedure analogous to example 17. 1H NMR (400 MHz, DMSO) d 11.1 (s, 2H), 8.27 (d, 1H), 7.73 (s, 1H), 7.48 (m, 5H), 7.19 (m, 1), 7.03 (d, 1H), 6.50 (s, 1H); LC-MS: 348 (MH+); HPLC RT: 5.11 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492383B1
Source datasetuspto-grants-2002_12
ORD IDord-b3688f23300a4528bcf689bfbe199a33
Source noteuspto-grants-2002_12