Benzoyl chloride → HCID 136333648, compound

HRID 1005367Notes

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]CCCCCCCCC.C(Cl)(=O)C1C=CC=CC=1.C(Cl)(=O)CCCCCCCCCCCCCCC.C(=O)(O)[O-].[Na+]>>[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])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

Reactant 4

HCID 7412Benzoyl chloride

HCID 8206Palmitoyl chloride

HCID 516892Sodium Bicarbonate

HCID 136333583HCID 136333583, compound

Product 1

HCID 136333648HCID 136333648, compound

Procedure

This compound was prepared using the procedure for palmitoyl-2'-deoxyguanosine, substituting the appropriate amount of benzoyl chloride for palmitoyl chloride, and substituting a 1:1 mixture of ice water and saturated aqueous sodium bicarbonate solution in the workup.

Workup

customThis compound was prepared

Sources & evidence

ORD record: ord-82fe75e205514774b7b24632c6d3ab5a
Source dataset: uspto-grants-2000_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06054441

Reaction notes

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