HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270560Generated: October 27, 2026
Triethylamine → Ammonium hydroxide methanol
https://huagongshe.com/reaction/270560
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 3-Methyloxan-4-one | HCID 14170926 | — |
| Reactant | HCID 68930927 | HCID 68930927 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ammonium Hydroxide | HCID 14923 | — |
| Product | Ammonium hydroxide methanol | HCID 21894508 | 1% |
| Product | HCID 68597077 | HCID 68597077 | — |
Reaction Steps
To a solution of 1-{[(1S,3R)-3-amino-1-isopropylcyclopentyl]carbonyl}-4-[2-(trifluoromethyl)phenyl]piperidin-4-ol hydrochloride (50 mg, 0.1 mmol), 3-methyltetrahydro-4H-pyran-4-one (39 mg, 0.34 mmol), and triethylamine (0.048 mL, 0.34 mmol) in methylene chloride (5 mL) was added sodium triacetoxyborohydride (73 mg, 0.34 mmol). After being stirred overnight at room temperature, a saturated solution of NaHCO3 was added. The solution was extracted with methylene chloride three times. The combined extracts were dried (MgSO4), filtered, and concentrated. Purification by flash chromatography on silica gel (0-20% B over 15 min. Bottle A=1% NH4OH/2% MeOH/EtOAc, Bottle B=1% NH4OH/MeOH) afforded the desired product as an oil. MS calculated for C27H39F3N2O3: (M+H) 497; found 497.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07449467B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-16e8affef9cc44f090a7f58699380b36 |
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| Source note | uspto-grants-2008_11 |
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