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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575295Generated: October 30, 2026

Methyl iodide → Ethyl 9-bromo-4-(methoxymethyl)-4,5-dihydrobenzo[2,3]oxepino[4,5-d]thiazole-2-carboxylate

https://huagongshe.com/reaction/575295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl 9-bromo-4-(hydroxymethyl)-4,5-dihydrobenzo[2,3]oxepino[4,5-d]thiazole-2-carboxylateHCID 86693325—
CatalystSilver(II) oxideHCID 92152—
SolventDichloromethaneHCID 6344—
ProductEthyl 9-bromo-4-(methoxymethyl)-4,5-dihydrobenzo[2,3]oxepino[4,5-d]thiazole-2-carboxylateHCID 8669332653.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of ethyl 9-bromo-4-(hydroxymethyl)-4,5-dihydrobenzo[2,3]oxepino[4,5-d]thiazole-2-carboxylate (200 mg, 0.52 mmol, 1.00 equiv), MeI (750 mg, 5.28 mmol, 10.00 equiv) and silver oxide (480 mg, 2.07 mmol, 4.00 equiv) in dichloromethane (15 mL) was stirred for 6 h at 50° C. The solids were filtered out and the filtrate was concentrated under vacuum. The residue was purified by a silica gel column with ethyl acetate/petroleum ether (1:10) to give 110 mg (53%) of the titled compound as an off-white solid; LC-MS (ES, m/z) 398,400 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034866B2
Source datasetuspto-grants-2015_05
ORD IDord-7bd8e4a22d264f6d8be157b5e4035723
Source noteuspto-grants-2015_05