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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415282Generated: October 25, 2026

Cyanamide → [4-Amino-2-[4-(2-ethylamino-ethoxy)-phenylamino]-thiazol-5-yl]-benzo[1,3]dioxol-5-yl-methanone

https://huagongshe.com/reaction/2415282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanamideHCID 9864—
Reactant1-(1,3-Dioxaindan-5-yl)-2-bromoethan-1-oneHCID 243777—
ReactantEthyl-[2-(4-isothiocyanato-phenoxy)-ethyl]-carbamic acid tert-butyl esterHCID 23525784—
Product[4-Amino-2-[4-(2-ethylamino-ethoxy)-phenylamino]-thiazol-5-yl]-benzo[1,3]dioxol-5-yl-methanoneHCID 10477555—

Reaction Steps

This compound was prepared from cyanamide, ethyl-[2-(4-isothiocyanato-phenoxy)-ethyl]-carbamic acid tert-butyl ester of Example 129D and 1-benzo[1,3]dioxol-5-yl-2-bromoethanone (Example 132) following a procedure similar to Example 130. The crude product was purified by HPLC using a Waters Symmetry C-18 21.2×75 mm column with the following gradient: A (0.05% trifluoroacetic acid in water), B (0.035% trifluoroacetic acid in acetonitrile, A to B gradient (0 to 50% over 7 minutes) flow rate: 20 mL/minute. The recovered product was dissolved in ethyl acetate, washed with 0.05N aqueous sodium hydroxide, and then with water. The ethyl acetate was dried (Na2SO4), concentrated, and the resulting residue triturated with ether to yield the product. Mass spectrum (ES) MH+=427.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06818663B2
Source datasetuspto-grants-2004_11
ORD IDord-7116cd9769444783a67edad070152096
Source noteuspto-grants-2004_11