HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873971Generated: October 26, 2026
Water → Benzyl 2-(1-benzyl-3-cyclopropylindazol-6-yloxy)ethylcarbamate
https://huagongshe.com/reaction/1873971
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | benzyl N-(2-bromoethyl)carbamate | HCID 278694 | — |
| Reactant | 1-Benzyl-3-cyclopropylindazol-6-ol | HCID 135869942 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Benzyl 2-(1-benzyl-3-cyclopropylindazol-6-yloxy)ethylcarbamate | HCID 59370774 | — |
Reaction Steps
Benzyl 2-bromoethylcarbamate (1.0563 g) which can be prepared according to the method described in Reference example 40, etc. was dissolved in dehydrated DMF (5 mL), added with 1-benzyl-3-cyclopropylindazol-6-ol (533.4 mg) which can be prepared according to the method described in Reference example 3, etc. and potassium carbonate (879.1 mg), and stirred overnight at 50° C. under nitrogen atmosphere. After cooling to room temperature, the reaction solution was added to water and extraction was carried out twice with ethyl acetate. The organic layer was washed twice with water and once with brine and dried over sodium sulfate. After the solvent was evaporated under reduced pressure, the resulting reside was purified by column chromatography (“COLUMN-B”; n-hexane:ethyl acetate=81:19→60:40) to obtain the title compound as a crude product (508.2 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304443B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-cfac119e45ad4e9f8922ddc737d836a9 |
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| Source note | uspto-grants-2012_11 |
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