Carbon Dioxide → HCID 86744844, compound

HRID 1493657Notes

Reaction equation

HRID 1493657 reaction equation
[CH3:1][C:2]1[C:8](=[O:9])[C:7]2[N:10]3[C@@:14]([O:21][CH3:22])([C@H:15]([CH2:16][O:17][C:18]([NH2:20])=[O:19])[C:6]=2[C:4](=[O:5])[C:3]=1[O:24][CH3:25])[C@H:13]1[NH:23][C@H:12]1[CH2:11]3.[OH-].[K+].C(=O)=O.[O:31]([CH2:38]CO)[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1>CCOCC>[C:18](=[O:17])([OH:19])[NH2:20].[OH:17][CH2:16][CH:15]1[C:6]2[C:4](=[O:5])[C:3]([O:24][CH2:25][CH2:38][O:31][C:32]3[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=3)=[C:2]([CH3:1])[C:8](=[O:9])[C:7]=2[N:10]2[CH2:11][CH:12]3[NH:23][CH:13]3[C:14]12[O:21][CH3:22]

Participants

6

Procedure

A solution of mitomycin A (100 mg) in 2 l of 2-phenoxyethanol was stirred at room temperature under nitrogen for 45 minutes with 500 mg of a 1.6% solution of KOH in 2-phenoxyethanol. The reaction product was diluted with ether then decomposed with dry ice. Components of etherial solution were separated on a silica gel column using triethylamine, which elutes the 2-phenoxyethanol, and then a mixture of chloroform and methanol 9:1, which elutes the product. The product was further purified by preparative thin layer chromatography on silica gel with a mixture of chloroform and acetone 6:4. This procedure gave 93 mg (71%) of the title compound, having a melting point of 153°-155° C. and providing the following analysis:

Workup

  1. customComponents of etherial solution were separated on a silica gel column
  2. additiona mixture of chloroform and methanol 9:1, which
  3. customThe product was further purified by preparative thin layer chromatography on silica gel with a mixture of chloroform and acetone 6:4

Sources & evidence

ORD record
ord-014fa88cc6a24ec1961911d60e7f1af3
Source dataset
uspto-grants-1991_06
Patent number
US05023253

Reaction notes

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