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Isoamyl Nitrite → Z-Ser-Leu-Ser-OCH3

HRID 1632419
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1632419
[NH:1]([C:9]([O:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:10])[C@H:2]([C:5]([NH:7]N)=[O:6])[CH2:3][OH:4].Cl.O1CCOCC1.N(OCCC(C)C)=O.[N-]=[N+]=[N-].N[C@H:38]([C:43]([NH:45][C@H:46]([C:49]([O:51][CH3:52])=[O:50])[CH2:47][OH:48])=[O:44])[CH2:39][CH:40]([CH3:42])[CH3:41].Cl>CN(C)C=O.NN.O.C(N(CC)CC)C>[NH:1]([C:9]([O:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:10])[C@H:2]([C:5]([NH:7][C@H:38]([C:43]([NH:45][C@H:46]([C:49]([O:51][CH3:52])=[O:50])[CH2:47][OH:48])=[O:44])[CH2:39][CH:40]([CH3:42])[CH3:41])=[O:6])[CH2:3][OH:4]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

10

Edukt 5

HCID 8053Isoamyl NitriteHCID 33558AzideHCID 7016357(S)-Benzyl (1-hydrazinyl-3-hydroxy-1-oxopropan-2-yl)carbamateHCID 13875640H-Leu-Ser-OCH3.HClHCID 204431481,4-Dioxane hydrochloride

Produkt 1

HCID 91978513Z-Ser-Leu-Ser-OCH3

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 962WaterLösungsmittelHCID 6228DimethylformamideLösungsmittel3×HCID 8471TriethylamineLösungsmittel2×HCID 9321HydrazineLösungsmittel

Reaktionsbedingungen

Temperatur
-15 °C

Versuchsvorschrift

3.19 Grams of Z-Ser-NHNH2 was dissolved in 25 ml of dimethylformamide, and 6.30 ml of 6N-hydrochloric acid/dioxane was added to the solution, cooled to -15° C., then 1.69 ml of isoamyl nitrite was added thereto. After the reaction mixture shows a negative reaction in hydrazine-test, 1.76 ml of a cold dimethylformamide solution with 5.29 ml of triethylamine was added drop by drop in small amount to neutralize the reaction mixture. This reaction mixture containing an azide product was added to 20 ml of a cold dimethylformamide solution containing H-Leu-Ser-OCH3.HCl obtained in the above-mentioned step 14(a) and 1.60 ml of triethylamine, and the whole mixture was stirred at -10° to -15° C. for 2 hours, next at 4° C. for 18 hours. Dimethylformamide was removed by distillation under a reduced pressure, the residue obtained was solidified by adding water, reprecipitated from methanol-ethyl acetate to obtain 4.11 g of the desired product.

Aufarbeitung

  1. additionwas added drop by drop in small amount
  2. customDimethylformamide was removed by distillation under a reduced pressure
  3. customthe residue obtained
  4. customreprecipitated from methanol-ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-a293f166da0540ffa1c432bcd83609e3
Quelldatensatz
uspto-grants-1984_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04474754

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