HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295362Generated: October 31, 2026
Hydrochloric Acid → HCID 178483321, compound
https://huagongshe.com/reaction/1295362
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | (1S,2S)-1-(3,5-Bis-trifluoromethyl-benzyloxymethyl)-2-phenyl-3-aza-bicyclo[3.1.0]hexane | HCID 86602046 | — |
| Reactant | HCID 178483326 | HCID 178483326 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 178483321 | HCID 178483321 | 66% |
Reaction Steps
To racemic Intermediate 24, one enantiomer being (1S,2S)-1-(3,5-bis-trifluoromethyl-benzyloxymethyl)-2-phenyl-3-aza-bicyclo[3.1.0]hexane (0.08 g, 0.18 mmol) in DME (1.0 mL) was added 5-dimethylaminomethyl-1H-[1,2,3]triazole-4-carbaldehyde (˜50% pure, 0.14 g, 0.91 mmol) and the mixture stirred at room temperature for 3 hours. To the reaction flask was added sodium triacetoxyborohydride (0.08 g, 0.36 mmol) and stirring was continued for 16 hours. To the reaction flask was added 1 N HCl (2 mL) and the mixture stirred for 2 hours. 1 N NaOH solution was added cautiously and then saturated sodium bicarbonate solution was added until the pH=8. The reaction mixture was extracted with methylene chloride, the organics washed with brine, dried over sodium sulfate, filtered, and concentrated. The crude product was purified by flash chromatography using elution of a gradient of 50% EtOAc/Hexanes to 3% MeOH/EtOAc to give the title compound. (0.065 g, 66% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07241798B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-8be32a0854e94a4dab5907a686879e75 |
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| Source note | uspto-grants-2007_07 |
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