HCID 86735652, compound → HCID 86735651, compound

HRID 2083798Notes

Reaction equation

HRID 2083798 reaction equation
[P:1]([O:9][CH2:10][C@H:11]1[O:15][C@@H:14]([N:16]2[CH:38]=[CH:37][C:20]([NH:21][C:22](=[O:36])[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH3:35])=[N:19][C:17]2=[O:18])[C@H:13]([OH:39])[C@@H:12]1[OH:40])([O:4]P(O)(O)=O)(=[O:3])[OH:2].P(OC[C@H]1O[C@@H](N2C=CC(NC(=O)CCCCCCCCCCCCCC)=NC2=O)[C@H](O)[C@@H]1O)(OP(O)(O)=O)(=O)O.P(OC[C@H]1O[C@@H](N2C=CC(NC(=O)CCCCCCCCCCCCCCC)=NC2=O)[C@H](O)[C@@H]1O)(OP(O)(O)=O)(=O)O.P(OC[C@H]1O[C@@H](N2C=CC(NC(=O)CCCCCCCCCCCCCCCC)=NC2=O)[C@H](O)[C@@H]1O)(OP(O)(O)=O)(=O)O.P(OC[C@H]1O[C@@H](N2C=CC(NC(=O)CCCCCCCCCCCCCCCCC)=NC2=O)[C@H](O)[C@@H]1O)(OP(O)(O)=O)(=O)O.P(OC[C@H]1O[C@@H](N2C=CC(NC(=O)CCCCCCCCCCCCCCCCCC)=NC2=O)[C@H](O)[C@@H]1O)(OP(O)(O)=O)(=O)O.P(OC[C@H]1O[C@@H](N2C=CC(NC(=O)CCCCCCCCCCCCCCCCCCC)=NC2=O)[C@H](O)[C@@H]1O)(OP(O)(O)=O)(=O)O.P(OC[C@H]1O[C@@H](N2C=CC(NC(=O)CCCCCCCCCCCCCCCCCCCC)=NC2=O)[C@H](O)[C@@H]1O)(OP(O)(O)=O)(=O)O.P(OC[C@H]1O[C@@H](N2C=CC(NC(=O)CCCCCCCCCCCCCCCCCCCCC)=NC2=O)[C@H](O)[C@@H]1O)(OP(O)(O)=O)(=O)O.P(OC[C@H]1O[C@@H](N2C=CC(NC(=O)CCCCCCC/C=C\CCCCCCCC)=NC2=O)[C@H](O)[C@@H]1O)(OP(O)(O)=O)(=O)O>>[P:1]([O:9][CH2:10][C@H:11]1[O:15][C@@H:14]([N:16]2[CH:38]=[CH:37][C:20]([NH:21][C:22](=[O:36])[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH3:35])=[N:19][C:17]2=[O:18])[C@H:13]([OH:39])[C@@H:12]1[OH:40])([OH:3])([OH:4])=[O:2]

Participants

11

Reactant 10

HCID 86735652HCID 86735652, compoundHCID 86735653HCID 86735653, compoundHCID 86735654HCID 86735654, compoundHCID 86735655HCID 86735655, compoundHCID 86735656HCID 86735656, compoundHCID 86735657HCID 86735657, compoundHCID 86735658HCID 86735658, compoundHCID 86735659HCID 86735659, compoundHCID 86735660HCID 86735660, compoundHCID 86735661HCID 86735661, compound

Product 1

HCID 86735651HCID 86735651, compound

Procedure

Also, the following the above procedure using N4 -myristoylcytidine-5'-pyrophosphate, N4 -pentadecanoylcytidine-5'-pyrophosphate, N4 -palmitoylcytidine-5'-pyrophosphate, N4 -margaroylcytidine-5'-pyrophosphate, N4 -stearoylcytidine-5'-pyrophosphate, N4 -nonadecanoylcytidine-5'-pyrophosphate, N4 -arachidoylcytidine-5'-pyrophosphate, N4 -heneicosanoylcytidine-5'-pyrophosphate, N4 -behenoylcytidine-5'-pyrophosphate, and N4 -oleoylcytidine-5'-pyrophosphate, respectively, instead of N4 -myristoylcytidine-5'-phosphate, the following products were obtained:

Sources & evidence

ORD record
ord-53f55efa96204047b3ccd75c8901eb85
Source dataset
uspto-grants-1978_04
Patent number
US04086417

Reaction notes

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