HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117955Generated: October 27, 2026
Water → tert-Butyl{2-[(4-{2-[2-(acetylamino)-1,3-thiazol-4-yl]ethyl}phenyl)amino]ethyl}carbamate
https://huagongshe.com/reaction/2117955
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | tert-Butyl N-(2-bromoethyl)carbamate | HCID 4103526 | — |
| Reactant | N-{4-[2-(4-aminophenyl)ethyl]thiazol-2-yl}acetamide | HCID 21914814 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | tert-Butyl{2-[(4-{2-[2-(acetylamino)-1,3-thiazol-4-yl]ethyl}phenyl)amino]ethyl}carbamate | HCID 86595614 | — |
Reaction Steps
To a suspension of N-(4-[2-(4-aminophenyl)ethyl]-1,3-thiazol-2-yl}acetamide (100 mg) in toluene were added tert-butyl (2-bromoethyl)carbamate (87.5 mg) and N,N-diisopropylethylamine (52 μl), and the mixture was stirred at 80° C. for 24 h. The reaction mixture was allowed to cool to room temperature, water (10 ml) was added, and the organic layer was separated, washed with saturated aqueous NaCl, dried over MgSO4, filtered, and concentrated in vacuo to give tert-butyl {2-[(4-{2-[2-(acetylamino)-1,3-thiazol-4-yl]ethyl}phenyl)amino]ethyl}carbamate as a pale brown amorphous.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07442715B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-af6eeb699df54d2fb06da7fe84513fee |
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| Source note | uspto-grants-2008_10 |
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