HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1512057Erstellt: 26. Oktober 2026
Acetic Acid → 4-{2-[2-Methyl-4-((2S,3'S)-2-methyl-[1,3']bipyrrolidinyl-1'-yl)-phenylamino]-ethyl}-tetrahydro-pyran-4-carboxylic acid methyl ester
https://huagongshe.com/reaction/1512057
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Edukt | Ammonia methanol | HCID 21705897 | — |
| Edukt | methyl 4-(2-oxoethyl)tetrahydro-2H-pyran-4-carboxylate | HCID 58468045 | — |
| Edukt | 2-methyl-4-(2-(S)-methyl-[1,3'(S)]bipyrrolidinyl-1'-yl)-phenylamine | HCID 59401764 | — |
| Lösungsmittel | 1,2-Dichloroethane | HCID 11 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Ammonia methanol | HCID 21705897 | — |
| Produkt | 4-{2-[2-Methyl-4-((2S,3'S)-2-methyl-[1,3']bipyrrolidinyl-1'-yl)-phenylamino]-ethyl}-tetrahydro-pyran-4-carboxylic acid methyl ester | HCID 67423255 | 119,5% |
Reaktionsschritte
2-Methyl-4-((2S,3′S)-2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenylamine (4.56 mmol) was dissolved in DCE (20 mL); to this solution was transferred a solution of 4-(2-Oxo-ethyl)-tetrahydro-pyran-4-carboxylic acid methyl ester (0.85 g, 4.56 mmol) in DCE (50 mL). To this clear solution was then added acetic acid (0.86 g, 14.3 mmol, 3.1 equiv), followed by addition of powder NaBH(OAc)3 (CSN: 56553-60-7, mw=211.94): 2.9 g, 13.6 mmol, 3 equiv.) in one portion under N2 at r.t. The yellowish milky solution was stirred at r.t. overnight. LC/MS showed m/z 429.35/430.40 at t=2.123 min. TLC (5% of 7N NH3/MeOH in DCM) showed no SM. The reaction was diluted with DCM (40 mL) and quenched with 30 mL of conc. NH4OH in 70 mL of water. The two layers were separated, and the aqueous layer was extracted with DCM (10 mL×2). The combined DCM extracts were washed with sodium bicarbonate (10 mL), and brine (15 mL), dried (anhydrous potassium carbonate), filtered, and concentrated. The product was purified on a 25 g-silica gel column (0-20%, 0-4 min; 20-40: 4-13 min; 40%: 13-25 min (A is % of 7N NH3/MeOH in DCM) to get 1.17 g (60%) of the title compound as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08217052B2 |
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| Quelldatensatz | uspto-grants-2012_07 |
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| ORD ID | ord-f2a79ca6e55647acbaaadd3fbf200f40 |
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| Quellennotiz | uspto-grants-2012_07 |
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