HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromomethyl 2-methoxyphenyl ketone → HCID 178462471, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromomethyl 2-methoxyphenyl ketone | HCID 123440 | — |
| Reactant | 4-(3-Ethylthioureido)benzenesulfonic acid | HCID 58349847 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178462471 | HCID 178462471 | — |
Reaction Steps
A solution of 4-(3-ethylthioureido)benzenesulfonic acid (1-4) (50 mg, 0.19 mmol) and 2-bromo-1-(2-methoxyphenyl)ethanone (30 mg, 0.13 mmol) in MeOH (1 mL) is heated to 80° C. for 1 hour and then cooled to room temperature and concentrated. The residual is purified by preparative LC/MS to provide (Z)-4-(3-ethyl-4-(2-methoxyphenyl)thiazol-2(3H)-ylideneamino)benzenesulfonic acid (1-5) as white solid. HPLC-MS calculated for C18H18N2O4S2 (M+H+) 391.1. found 391.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08362050B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-e3e2a7cd256e4292b6dce6a2b8549d3a |
| Source note | uspto-grants-2013_01 |