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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyanamide | HCID 9864 | — |
| Reactant | 1-(1,3-Dioxaindan-5-yl)-2-bromoethan-1-one | HCID 243777 | — |
| Reactant | Ethyl-[2-(4-isothiocyanato-phenoxy)-ethyl]-carbamic acid tert-butyl ester | HCID 23525784 | — |
| Product | [4-Amino-2-[4-(2-ethylamino-ethoxy)-phenylamino]-thiazol-5-yl]-benzo[1,3]dioxol-5-yl-methanone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06818663B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-7116cd9769444783a67edad070152096 |
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| Source note | uspto-grants-2004_11 |
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