HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 476227Erstellt: 23. Oktober 2026
Formate → (R)-propyl 2-(7-amino-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-yl)acetate
https://huagongshe.com/de/reaction/476227
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Formate | HCID 283 | — |
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Pyridoxal 5'-phosphate | HCID 1051 | — |
| Edukt | Trisodium Phosphate | HCID 24243 | — |
| Edukt | D-Alanine | HCID 71080 | — |
| Edukt | Lactate | HCID 91435 | — |
| Edukt | Nadh | HCID 439153 | — |
| Edukt | Sodium Formate | HCID 2723810 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | (R)-propyl 2-(7-amino-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-yl)acetate | HCID 58349691 | 80% |
Reaktionsschritte
Sodium phosphate, dibasic (3.8 equiv.) and sodium formate (266 equiv.) were added to a solution of D-alanine (38 equiv.) in water. The pH was measured as 7.6. NAD (0.04 equiv.), Pyridoxal-5-phosphate (0.11 equiv.), Lactate dehydrogenase (LDH) (1 equiv.), Formate dehydrogenase (FDH) (1 equiv.), and Amine-Transaminase ATA117 (1 equiv.) were added under stirring and slowly dissolved. The measured pH was 7.3. The mixture was aged at 22° C. for 1 h. The flask was flushed with nitrogen and propyl (7-oxo-6,7,8,9-tetrahydropyrido[1,2-a]-indol-10-yl)acetate from Step 5 was added as a DMSO (0.06 M) solution. The reaction was adjusted to pH 7.2 and aged at 30° C. overnight under nitrogen atmosphere. Upon completion of the reaction as determined by HPLC, the pH of the reaction was adjusted to pH 4.0 with 6N HCl and Celite (20 g per L) was added. After stirring for 1 hr the reaction was filtered through a Celite bed and the filter cake was washed twice with 0.1N HCl. The combined aqueous filtrate was extracted with 1 volume of MTBE. The organic layer did not contain amine and was discarded. The aqueous layer was diluted with an equal volume of MTBE and the pH of the mixture was adjusted to pH 9.5 using 5N NaOH. The two phases were separated and the aqueous layer was extracted with MTBE. The spent aqueous layer had no detectable amine and was discarded. The combined organic layers were washed with dilute sodium carbonate and dried over Na2SO4. Evaporation of the volatiles afforded the crude title compound (80%). The ee was determined as 99% by SFC assay.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08637671B2 |
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| Quelldatensatz | uspto-grants-2014_01 |
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| ORD ID | ord-8723912062624398ba70fdb5dfdb76d6 |
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| Quellennotiz | uspto-grants-2014_01 |
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