HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1770Erstellt: 23. Oktober 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → (+/-)-(3aR*,8aS*)-1,2,3,3a,8,8a-Hexahydro-1,3a,8-trimethylpyrrolo-[2,3-b]indol-4-yl (R)-(alpha-methylbenzyl)carbamate
https://huagongshe.com/de/reaction/1770
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Edukt | alpha-Methylbenzyl isocyanate | HCID 85760 | — |
| Edukt | cis-(+/-)-1,2,3,3a,8,8a-Hexahydro-1,3a,8-trimethylpyrrolo [2,3-b]indol-4-ol | HCID 88402553 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (+/-)-(3aR*,8aS*)-1,2,3,3a,8,8a-Hexahydro-1,3a,8-trimethylpyrrolo-[2,3-b]indol-4-yl (R)-(alpha-methylbenzyl)carbamate | HCID 53984692 | — |
Reaktionsschritte
cis-(±)-1,2,3,3a,8,8a-Hexahydro-1,3a,8-trimethylpyrrolo [2,3-b]indol-4-ol (2g) was dissolved in degassed THF (200 ml). DBU (0.8 ml) was added to the mixture followed by R-(+)-α-methylbenzyl isocyanate (2 g). The reaction was stirred at room temperature overnight under nitrogen. The solvent was evaporated under reduced pressure and the residue was purified using Prep 500 chromatography (4% MeOH/DCM) to yield 1.2 g of a solid. This material was combined with 600 mg of identically prepared material, which was found to be pure by thin layer analysis. The combined product was triturated with isopropyl ether and filtered to yield 1.8 g of (±)-(3aR*, 8aS*)-1,2,3,3a,8,8a-hexahydro-1,3a,8-trimethylpyrrolo [2,3-b]indol-4-yl (R)-(α-methylbenzyl)carbamate, m.p. 151°-155° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05726323 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-cb9d1bc99b9b4ab18c65744a87225d92 |
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| Quellennotiz | uspto-grants-1998_03 |
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