HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642763Generated: November 2, 2026
1,2-Dichloroethane → HCID 58017527, compound
https://huagongshe.com/reaction/1642763
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | HCID 57473410 | HCID 57473410 | — |
| Reactant | HCID 58017546 | HCID 58017546 | — |
| Reactant | HCID 178418300 | HCID 178418300 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58017527 | HCID 58017527 | 87.3% |
Reaction Steps
To a solution of 2-tert-butyl 3-ethyl (3S)-isoxazolidine-2,3-dicarboxylate (245 mg, 1.00 mmol) in acetonitrile (2.5 mL) and water (1 mL) was added lithium hydroxide (1 M in water, 1.00 mL, 1.00 mmol) and the mixture was stirred at rt for 30 min. To this solution was added 5-chloro-2-tetrazol-1-yl-benzylamine hydrochloride (295 mg, 1.20 mmol, prepared as described in J. Med. Chem. 2004, 47, 2995), hydroxybenzotriazole (135 mg, 1.00 mmol, as a 20% solution in water, ca 0.65 mL), EDC (288 mg, 1.50 mmol) and NMM (202 mg, 2.00 mmol). The resulting mixture was stirred at rt over night, then diluted with DCM and washed with 1 M HCl and saturated sodium hydrogen carbonate. The organic phase was dried, filtered, evaporated and purified by flash chromatography (DCM/EtOAc gradient from 4:1 to 1:1) to give tert-butyl (3S)-3-{[5-chloro-2-(1H-tetrazol-1-yl)benzyl]carbamoyl}isoxazolidine-2-carboxylate (357 mg, 87%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08119673B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-b4e73c52171e4651b39f74f4fc2f4cb8 |
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| Source note | uspto-grants-2012_02 |
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