Mitoxantrone → HCID 12888484, compound

HRID 65397Notes

Reaction equation

HRID 65397 reaction equation
[OH:1][CH2:2][CH2:3][NH:4][CH2:5][CH2:6][NH:7][C:8]1[C:21]2[C:20](=[O:22])[C:19]3[C:14](=[C:15]([OH:24])[CH:16]=[CH:17][C:18]=3[OH:23])[C:13](=[O:25])[C:12]=2[C:11]([NH:26][CH2:27][CH2:28][NH:29][CH2:30][CH2:31][OH:32])=[CH:10][CH:9]=1.[F:33][C:34]([F:41])([F:40])[C:35]([O:37]CC)=O>CO>[OH:1][CH2:2][CH2:3][N:4]([CH2:5][CH2:6][NH:7][C:8]1[C:21]2[C:20](=[O:22])[C:19]3[C:14](=[C:15]([OH:24])[CH:16]=[CH:17][C:18]=3[OH:23])[C:13](=[O:25])[C:12]=2[C:11]([NH:26][CH2:27][CH2:28][N:29]([CH2:30][CH2:31][OH:32])[C:35](=[O:37])[C:34]([F:33])([F:40])[F:41])=[CH:10][CH:9]=1)[C:35](=[O:37])[C:34]([F:41])([F:40])[F:33]

Participants

4

Procedure

A suspension of 1.50 g. of 1,4-bis[2-(2-hydroxyethylamino)ethylamino]-5,8-dihydroxyanthraquinone in 75 ml. of ethyl triflouroacetate and 75 ml. of methanol is stirred for 10 minutes. Evaporation of the resulting solution in vacuo at 30° C. leaves a residue which is washed and macerated with methylene chloride, giving 2.11 g. of blue-black solid, m.p. 162° C.

Workup

  1. additionA suspension of 1.50 g
  2. customEvaporation of the resulting solution in vacuo at 30° C.
  3. customleaves a residue which
  4. washis washed
  5. customgiving 2.11 g

Sources & evidence

ORD record
ord-48206580251c4729804a8194d5b84042
Source dataset
uspto-grants-1986_09
Patent number
US04614618

Reaction notes

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