HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333310Generated: October 28, 2026
1-Hydroxybenzotriazole → HCID 178520375, compound
https://huagongshe.com/reaction/333310
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 1-(2-(Benzyloxy)-2-oxoethyl)cyclopentanecarboxylic acid | HCID 59608226 | — |
| Reactant | HCID 178511761 | HCID 178511761 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178520375 | HCID 178520375 | 39% |
Reaction Steps
To a suspension of 1-(2-(benzyloxy)-2-oxoethyl)cyclopentanecarboxylic acid (197 mg, 0.750 mmol) in THF (8 ml) at room temperature was added EDC.HCl (192 mg, 1.000 mmol) and HOBT (134 mg, 0.875 mmol). The mixture was stirred at room temperature for 10 minutes and was added a solution of (S)-2-(3′-chlorobiphenyl-4-yl)-1-(1H-tetrazol-5-yl)ethanamine (187 mg, 0.625 mmol) in THF and TEA (0.174 ml, 1.250 mmol). The mixture was stirred overnight at room temperature. The reaction was quenched by brine and was extracted with EtOAc. The combined organic layer was washed with brine and dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The obtained residue was purified by flash chromatography (silica gel, 1 to 3% EtOH/DCM) and gave the title compound: 134 mg (yield: 39%). LCMS (condition B): 544.3 (M+1); retention time=1.44 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877815B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-e5a4dd9fbc59496a85eb71c484f5ca2f |
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| Source note | uspto-grants-2014_11 |
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