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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2078834Generated: November 3, 2026

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

https://huagongshe.com/reaction/2078834

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 numberUS07928248B2
Source datasetuspto-grants-2011_04
ORD IDord-2570c11da1464fcf8bb9166051e59054
Source noteuspto-grants-2011_04