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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 12238Erstellt: 24. Oktober 2026

Glyoxylic Acid → [(S)-5-(6-Chloro-9H-beta-carbolin-8-ylcarbamoyl)-2,2-dimethyl-morpholin-4-yl]-acetic acid

https://huagongshe.com/de/reaction/12238

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktGlyoxylic AcidHCID 760—
EduktTriethylamineHCID 8471—
EduktSodium cyanoborohydrideHCID 5003444—
Edukt(S)-6,6-Dimethyl-morpholine-3-carboxylic acid (6-chloro-9H-beta-carbolin-8-yl)-amideHCID 67165625—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt[(S)-5-(6-Chloro-9H-beta-carbolin-8-ylcarbamoyl)-2,2-dimethyl-morpholin-4-yl]-acetic acidHCID 1138451272%

Reaktionsschritte

To a suspension of (S)-6,6-Dimethyl-morpholine-3-carboxylic acid (6-chloro-9H-beta-carbolin-8-yl)-amide (2.6 g, 6.0 mmoles) in 60 ml of methanol was added 1.7 ml of triethylamine (2.0 eq.), sodium cyanoborohydride (575 mg, 9.1 mmoles) and glyoxylic acid (780 mg, 8.5 mmoles). The reaction mixture was stirred at ambient temperature for 1.5 hrs. Water was added (5 ml) and the mixture was concentrated to a thick yellow slurry. More water was then added (30 ml) and the resulting slurry was stirred at ambient temperature for 10 min. and was filtered. The collected yellow solid was washed with water and dried under high vacuum to give 1.80 g (71%) of the desired product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07727985B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-5063a34e8e444b9699047499e466ff58
Quellennotizuspto-grants-2010_06