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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575095Generated: October 30, 2026

10-Bromo-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxamide → 10-[(7-hydroxy-6,7-dihydro-5H-cyclopenta[b]pyridin-7-yl)ethynyl]-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2-carboxamide

https://huagongshe.com/reaction/575095

Reaction equation

Participants

RoleNameHCIDCharge
Reactant10-Bromo-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxamideHCID 68312883—
Reactant7-ethynyl-6,7-dihydro-5H-cyclopenta[b]pyridin-7-olHCID 86669578—
Product10-[(7-hydroxy-6,7-dihydro-5H-cyclopenta[b]pyridin-7-yl)ethynyl]-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2-carboxamideHCID 71715450—

Reaction Steps

The title compound was prepared similarly according to Procedure E by reacting 10-bromo-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2-carboxamide with 7-ethynyl-6,7-dihydro-5H-cyclopenta[b]pyridin-7-ol. 1H NMR (500 MHz, DMSO) δ 2.30-2.43 (1H, m), 2.54-2.61 (1H, m), 2.83-2.95 (1H, m), 2.96-3.07 (1H, m), 4.49 (4H, s), 6.21 (1H, br. s.), 7.03 (1H, d, J=8.51 Hz), 7.14 (1H, br. s.), 7.24-7.36 (2H, m), 7.57 (1H, br. s.), 7.73 (1H, d, J=7.41 Hz), 7.80 (1H, s), 8.46 (1H, d, J=4.26 Hz), 8.53 (1H, d, J=2.05 Hz); LC-MS: m/z=387.10 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034866B2
Source datasetuspto-grants-2015_05
ORD IDord-26d264d14313428eba2a2b01d63e1281
Source noteuspto-grants-2015_05