Hydrochloric Acid → Ethyl 3-(4-(2-tetrazolyl)-phenylhydrazino)-4-oxopentanoate

HRID 1584746

Reaktionsgleichung

Reaktionsgleichung von HRID 1584746
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[N:12]=[N:11][CH:10]=[N:9]2)=[CH:4][CH:3]=1.Cl.[N:14]([O-])=O.[Na+].[C:18]([CH:21](C(=O)C)[CH2:22][C:23]([O:25][CH2:26][CH3:27])=[O:24])(=[O:20])[CH3:19]>C(O)C.N1C=CC=CC=1.O>[N:9]1[N:8]([C:5]2[CH:4]=[CH:3][C:2]([NH:1][NH:14][CH:21]([C:18](=[O:20])[CH3:19])[CH2:22][C:23]([O:25][CH2:26][CH3:27])=[O:24])=[CH:7][CH:6]=2)[N:12]=[N:11][CH:10]=1

Komponenten

8

Versuchsvorschrift

A solution of 1.06 gm. (6.58 mmoles) of 2-(4-aminophenyl)tetrazole in 20 ml. of ethanol and 1.18 ml. of concentrated hydrochloric acid and 10 ml. of water was cooled in an ice bath and treated dropwise with a solution of 500 mg. of sodium nitrite in 10 ml. of water. After the addition of an additional 10 ml. of water, the mixture was stirred for 25 minutes at room temperature. The mixture was then added to a solution of 1.35 gm. (7.2 mmoles) of ethyl 3-acetyl-4-oxopentanoate and 2.66 ml. of pyridine in 15 ml. of ethanol. A solid began to separate. After 1 hour, 10 ml. of 1M hydrochloric acid was added to adjust the pH to 2-3. An additional 50 ml. of water was added and the solid was collected and washed thoroughly with water and dried. 1.74 g. was obtained.

Aufarbeitung

  1. additiontreated dropwise with a solution of 500 mg
  2. additionAfter the addition of an additional 10 ml
  3. additionThe mixture was then added to a solution of 1.35 gm
  4. customto separate
  5. additionof 1M hydrochloric acid was added
  6. additionof water was added
  7. customthe solid was collected
  8. washwashed thoroughly with water
  9. customdried
  10. customwas obtained

Quellen und Nachweise

ORD-Eintrag
ord-3ef54fa340c74e2ea82c282c36704712
Quelldatensatz
uspto-grants-1999_08
Patentnummer
US05935957

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