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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627893Generated: October 26, 2026

Water → 2-Bromo-4,5-dihydropyrido[4,3-b]thieno[2,3-d]oxepine

https://huagongshe.com/reaction/627893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
Reactant4,5-Dihydropyrido[4,3-b]thieno[2,3-d]oxepineHCID 57900199—
SolventDimethylformamideHCID 6228—
Product2-Bromo-4,5-dihydropyrido[4,3-b]thieno[2,3-d]oxepineHCID 5790009165.4%

Reaction Steps

N-Bromosuccinimide (0.237 g, 1.33 mmol) in dimethylformamide (4 mL) was added dropwise to a solution of 4,5-dihydropyrido[4,3-b]thieno[2,3-d]oxepine (0.250 g, 1.23 mmol) in dimethylformamide (4 mL, 100 mmol) at 0° C. The reaction mixture was stirred for 18 hours at room temperature. The reaction mixture was mixed with 40 ml of water and extracted with 20 ml of ethylacetate twice. Combined organic extracts were washed with water and brine, and dried over MgSO4. The solvent was evaporated affording 2-bromo-4,5-dihydropyrido[4,3-b]thieno[2,3-d]oxepine (0.227 g, 63%). 1H NMR (500 MHz, CDCl3) δ 8.76 (s, 1H), 8.26 (d, J=5.4, 1H), 6.90 (d, J=5.5, 1H), 6.88 (s, 1H), 4.36 (t, J=4.7, 2H), 3.19 (t, J=4.8, 2H). MS (ESI+) 282.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309265B2
Source datasetuspto-grants-2016_04
ORD IDord-48c1d1002cc34fddb4ff3b6f431aef09
Source noteuspto-grants-2016_04