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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 613216Erstellt: 26. Oktober 2026

Diisopropylcarbodiimide → HCID 54181953, Verbindung

https://huagongshe.com/reaction/613216

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylcarbodiimideHCID 12734—
EduktTris(2-aminoethyl)amineHCID 77731—
EduktN-HydroxysuccinimideHCID 80170—
EduktN9-(t-butoxycarbonyl)-N6,N9-bis(2-methyl-2-triphenylmethylthiopropyl)-6,9-diazanonanoic acidHCID 53724287—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 54181953HCID 54181953—

Reaktionsschritte

BAT-BM was prepared as follows. BAT acid (N9 -(t-butoxycarbonyl)-N6,N9 -bis(2-methyl-2-triphenylmethylthiopropyl)-6,9-diazanonanoic acid) (10.03 g, 10.89 mmol) and 75 mL of dry methylene chloride (CH2Cl2) were added to a 250 mL round-bottomed flask equipped with magnetic stir bar and argon balloon. To this solution was added diisopropylcarbodiimide (3.40 mL, 21.7 mmol, 199 mole %), followed by N-hydroxysuccinimide (3.12g, 27.1 mmol, 249 mole %). This solution was observed to become cloudy within 1 h, and was further incubated with stirring for a total of 4 h at room temperature. A solution of tris(2-aminoethyl)amine (30 mL, 200 mmol, 1840 mole %) in 30 mL methylene chloride was then added and stirring continued overnight. The reaction mixture was then concentrated under reduced pressure, and the residue partitioned between ethylacetate (150 mL) and 0.5M potassium carbonate (K2CO3 ; 150 mL). The organic layer was separated, washed with brine and concentrated to give the crude product N-[2-N',N'-bis(2-aminoethyl)aminoethyl)]-N9 -(t-butoxycarbonyl)-N6,N9 -bis(2-methyl-2-triphenylmethylthiopropyl)-6,9-diazanonanamide as a foam/oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06007792
Quelldatensatzuspto-grants-1999_12
ORD IDord-4ab80fdf31b048899b5e73bf88efd563
Quellennotizuspto-grants-1999_12