2-Hydroxy-7-pyrimidin-5-yl-cyclohepta-2,4,6-trien-1-one → 2,4,6-Cycloheptatrien-1-one, 2,3,5,7-tetrakis(acetyloxy)-

HRID 1368786Notes

Reaction equation

HRID 1368786 reaction equation
C1C=CC(=O)C(O)=C(C2C=NC=NC=2)C=1.C1C=CC(=O)C(O)=C(C2C=NC=NC=2)C=1.COC1C(=O)C(C2C=NC=NC=2)=CC=CC=1.[CH3:47][C:48]([O:50][C:51]1[CH:58]=[C:57]([O:59][C:60]([CH3:62])=[O:61])[C:55](=[O:56])[C:54]([O:63][C:64]([CH3:66])=[O:65])=[C:53]([O:67][C:68]([CH3:70])=[O:69])[CH:52]=1)=[O:49].C1C=CC(=O)C(O)=C(C2C=NC=NC=2)C=1>>[CH3:47][C:48]([O:50][C:51]1[CH:58]=[C:57]([O:59][C:60]([CH3:62])=[O:61])[C:55](=[O:56])[C:54]([O:63][C:64]([CH3:66])=[O:65])=[C:53]([O:67][C:68]([CH3:70])=[O:69])[CH:52]=1)=[O:49]

Participants

3

Reactant 2

HCID 107505172-Hydroxy-7-pyrimidin-5-yl-cyclohepta-2,4,6-trien-1-oneHCID 131723918SP10 SP11 SP12 SP10

Product 1

HCID 140190602,4,6-Cycloheptatrien-1-one, 2,3,5,7-tetrakis(acetyloxy)-

Procedure

And, if the obtained result at this step SP12 is yes, then the CPU 15 returns to the step SP10, and, after this time, repeats the loop of the steps SP10-SP11-SP12-SP10 until the negative result is obtained at the step SP12; in this way, the file data of all files which have been stored in the very “media set” and not yet copied are copied into the “media set” that is newly created.

Workup

  1. customnegative result

Sources & evidence

ORD record
ord-025bb7a3da534ecab6158b04aecc067e
Source dataset
uspto-grants-2003_06
Patent number
US06574704B1

Reaction notes

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