Octanoyl chloride → HCID 136333618, compound

HRID 969765Notes

Reaction equation

HRID 969765 reaction equation
[C:1]([C@@:18]1([N:26]2[C:36]3[N:35]=[C:33]([NH2:34])[NH:32][C:30](=[O:31])[C:29]=3[N:28]=[CH:27]2)[O:25][C@H:22]([CH2:23][OH:24])[C@@H:20]([OH:21])[CH2:19]1)(=[O:17])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]CCCCCCCC.C(Cl)(=O)CCCCCCC.C(Cl)(=O)CCCCCCCCCCCCCCC>>[C:1]([C@@:18]1([N:26]2[C:36]3[N:35]=[C:33]([NH2:34])[NH:32][C:30](=[O:31])[C:29]=3[N:28]=[CH:27]2)[O:25][C@H:22]([CH2:23][OH:24])[C@@H:20]([OH:21])[CH2:19]1)(=[O:17])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]

Participants

4

Reactant 3

HCID 8124Octanoyl chlorideHCID 8206Palmitoyl chlorideHCID 136333583HCID 136333583, compound

Product 1

HCID 136333618HCID 136333618, compound

Procedure

This compound was prepared using the procedure for palmitoyl-2′-deoxyguanosine, substituting the appropriate amount of octanoyl chloride for palmitoyl chloride.

Workup

  1. customThis compound was prepared

Sources & evidence

ORD record
ord-52da4acedc71443ebdd3c947afc975af
Source dataset
uspto-grants-2007_12
Patent number
US07307166B1

Reaction notes

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