Hydrazine hydrate (1:1) → HCID 53942049, compound

HRID 1769222Notes

Reaction equation

HRID 1769222 reaction equation
C1(=O)[N:5]([CH2:6][CH2:7][CH2:8][N:9]2[C:24](=[O:25])[C:23]([CH3:26])=[CH:22][N:11]([C@@H:12]3[O:18][C@H:15]([CH2:16][OH:17])[C@@H:14]([N:19]=[N+:20]=[N-:21])[CH2:13]3)[C:10]2=[O:27])C(=O)C2=CC=CC=C12.O.NN>CO>[NH2:5][CH2:6][CH2:7][CH2:8][N:9]1[C:24](=[O:25])[C:23]([CH3:26])=[CH:22][N:11]([C@@H:12]2[O:18][C@H:15]([CH2:16][OH:17])[C@@H:14]([N:19]=[N+:20]=[N-:21])[CH2:13]2)[C:10]1=[O:27]

Participants

4

Procedure

A solution of approximately 0.5 mmole 3-PHT-P-AZT (Example 26) methanol was treated with 50 ul hydrazine hydrate and incubated overnight at room temperature. The resulting suspension was filtered through a 0.45 um PTFE membrane and the filtrate chromatographed by preparative TLC on silica gel-F 2000 um using the solvent system CHCl3 /MeOH/15M NH4OH (85+15+1). The major band (Rf =0.27; UV positive; ninhydrin positive) was well separated from 3-PHT-P-AZT (Rf =0.78; UV positive; ninhydrin negative) and from hydrazine (Rf =0.0; UV negative; ninhydrin postive). The product was eluted with MeOH. It was found to be immunologically active in an AZT assay by FPIA, was homogeneous on analytical TLC and its UV spectrum resembled that of a 3-alkylated AZT derivative.

Workup

  1. filtrationThe resulting suspension was filtered through a 0.45 um PTFE membrane
  2. customthe filtrate chromatographed by preparative TLC on silica gel-F 2000 um
  3. customThe major band (Rf =0.27; UV positive; ninhydrin positive) was well separated from 3-PHT-P-AZT (Rf =0.78; UV positive; ninhydrin negative) and from hydrazine (Rf =0.0; UV negative; ninhydrin postive)
  4. washThe product was eluted with MeOH

Sources & evidence

ORD record
ord-9deb9876c6034bb58165719132e165ed
Source dataset
uspto-grants-1995_01
Patent number
US05380825

Reaction notes

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