HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484208Generated: November 2, 2026
1-Hydroxybenzotriazole → HCID 86714205, compound
https://huagongshe.com/reaction/1484208
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 12161723 | HCID 12161723 | — |
| Reactant | HCID 12599566 | HCID 12599566 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86714205 | HCID 86714205 | 181.7% |
Reaction Steps
The PNP-derivative 34 derived from the minor alcohol 31 (300 mg, 1.03 mmol) was dissolved in 10.3 g THF. Diisopropylethylamine (362 mg, 2.80 mmol) was added, followed by 1-hydroxybenzotriazole (75 mg, 0.556 mmol) and ethyl 2-(4-aminophenyl)-2-hydroxyacetate (325 mg, 1.67 mmol, prepared as described in WO 2009109998). The mixture was stirred in the dark at ca. 30° C. for 6 days. The solvent was removed by rotary evaporation and the residue was chromatographed on 21 g silica, using dichloromethane with gradually increasing amounts of TBME as the eluent. The product eluted with ca. 5% TBME. Rotary evaporation of the product fractions afforded minor (E)-ethyl 2-(4-(((cyclooct-2-en-1-yloxy)carbonyl)amino)phenyl)-2-hydroxyacetate (36) as a viscous oil (350 mg, 1.01 mmol, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09421274B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-b1dbfca4a5da4168b1933c0dea2bbf02 |
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| Source note | uspto-grants-2016_08 |
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