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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1949729Generated: November 3, 2026

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

https://huagongshe.com/reaction/1949729

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 numberUS08399690B2
Source datasetuspto-grants-2013_03
ORD IDord-883b448e1ff645cd8256e764e74c33a2
Source noteuspto-grants-2013_03