HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886988Generated: November 1, 2026
Sodium triacetoxyborohydride → HCID 178502916, compound
https://huagongshe.com/reaction/1886988
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 1-Methoxyphosphinan-4-one 1-oxide | HCID 11073732 | — |
| Reactant | HCID 67036200 | HCID 67036200 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178502916 | HCID 178502916 | 78.7% |
Reaction Steps
3-(N-(4-aminocyclohexyl)-4-methylcyclohexanecarboxamido)-5-(3,3-dimethylbut-1-ynyl)thiophene-2-carboxylic acid hydrochloride (40 mg, 0.083 mmol) and 1-methoxy-1-oxo-1λ5-phosphinan-4-one (27 mg, 0.166 mmol) were dissolved in 2 mL of DMF. Sodium triacetoxyborohydride (35 mg, 0.166 mmol) was added. The reaction mixture was allowed to stir at room temperature over 18 hours, and then diluted with EtOAc, washed with saturated sodium bicarbonate and brine. The organic layer was dried over magnesium sulfate, filtered and concentrated. The residue was purified by HPLC (Gemini column; 5% acetonitrile:water, 5 min; 5-100% acetonitrile:water, 18 min; 100% acetonitrile, 6 min; both solvents containing 0.1% trifluoroacetic acid) to give title compound (38.6 mg): MS (m/z): 591.3 [M+H]−; HPLC retention time: 3.28 min (2-98% acetonitrile:water with 0.05% trifluoroacetic acid).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501714B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-6066e5293fe94af2a3249dd67a30a674 |
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| Source note | uspto-grants-2013_08 |
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