HCID 613105, compound → HCID 86753928, compound

HRID 1418702Notes

Reaction equation

HRID 1418702 reaction equation
[OH:1][CH:2]([C:5]1[CH:21]=[C:20]2[N:8]([CH2:9][C:10]3[C:11]2=[N:12][C:13]2[C:18]([CH:19]=3)=[CH:17][CH:16]=[CH:15][CH:14]=2)[C:7](=[O:22])[C:6]=1[CH3:23])[CH2:3][CH3:4].[CH:24]1[C:36]2[CH:35]([CH2:37][O:38][C:39]([NH:41][CH2:42][P:43](=O)([OH:45])[OH:44])=[O:40])[C:34]3[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=3)[C:28]=2[CH:27]=[CH:26][CH:25]=1>O>[CH:33]1[C:34]2[CH:35]([CH2:37][O:38][C:39]([NH:41][CH2:42][P:43]([OH:45])([O:1][CH:2]([C:5]3[CH:21]=[C:20]4[N:8]([CH2:9][C:10]5[C:11]4=[N:12][C:13]4[C:18]([CH:19]=5)=[CH:17][CH:16]=[CH:15][CH:14]=4)[C:7](=[O:22])[C:6]=3[CH3:23])[CH2:3][CH3:4])=[O:44])=[O:40])[C:36]3[C:28](=[CH:27][CH:26]=[CH:25][CH:24]=3)[C:29]=2[CH:30]=[CH:31][CH:32]=1

Participants

4

Reactant 2

HCID 613105HCID 613105, compoundHCID 15339930HCID 15339930, compound

Product 1

HCID 86753928HCID 86753928, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

The title compound was prepared according to the procedure in Example 21 except using (±)-7-(1-hydroxypropyl)-8-methylindolizino[1,2-b]quinolin-9(11H)-one and [[[(9-fluorenylmethoxy)carbonyl]amino]methyl]phosphonic acid. Anal. Calcd for C35H32N3O6P.9/8 H2O: C, 65.49; H, 5.38; N, 6.55. Found: C, 65.83; H, 5.28; N, 6.14.

Sources & evidence

ORD record
ord-c585ec95271d4e009b4d3302fe408ca8
Source dataset
uspto-grants-1999_03
Patent number
US05883255

Reaction notes

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