Dicyclohexylcarbodiimide → HCID 131715158, compound

HRID 979445Notes

Reaction equation

HRID 979445 reaction equation
C1(N=C=NC2CCCCC2)CCCCC1.[NH2:16][CH2:17][CH2:18][C:19]1[NH:28][C:27]2[C:26](=[O:29])[N:24]([CH3:25])[C:23](=[O:30])[N:22]([CH3:31])[C:21]=2[N:20]=1.[CH:32]1[C:37]([C:38]([OH:40])=[O:39])=[CH:36][C:35]2[C:41]3([O:57][C:58](=[O:59])[C:34]=2[CH:33]=1)[C:51]1[CH:52]=[CH:53][C:54]([OH:56])=[CH:55][C:50]=1[O:49][C:43]1[CH:44]=[C:45]([OH:48])[CH:46]=[CH:47][C:42]3=1>N1C=CC=CC=1>[NH2:16][CH2:17][CH2:18][C:19]1[NH:28][C:27]2[C:26](=[O:29])[N:24]([CH3:25])[C:23](=[O:30])[N:22]([CH3:31])[C:21]=2[N:20]=1.[CH:32]1[C:37]([C:38]([OH:40])=[O:39])=[CH:36][C:35]2[C:41]3([O:57][C:58](=[O:59])[C:34]=2[CH:33]=1)[C:51]1[CH:52]=[CH:53][C:54]([OH:56])=[CH:55][C:50]=1[O:49][C:43]1[CH:44]=[C:45]([OH:48])[CH:46]=[CH:47][C:42]3=1

Participants

5

Reactant 3

HCID 10868DicyclohexylcarbodiimideHCID 768066-CarboxyfluoresceinHCID 4140301AC1N56UX

Product 1

HCID 131715158HCID 131715158, compound

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Procedure

N,N'-dicyclohexylcarbodiimide (15 mg) was added to a solution of 8-β-aminoethyltheophylline (5 mg) and carboxyfluorescein (5 mg) in 0.5 ml of pyridine. The reaction was allowed to proceed for two hours at room temperature and the reaction product was purified twice employing silica gel thin-layer chromatography using a thin chloroform:methanol (2:1) mixture as developing solvent to yield an 8-β-amino ethyltheophylline-carboxyfluorescein conjugate of the formula: ##STR10##

Workup

  1. customthe reaction product was purified twice employing silica gel thin-layer chromatography

Sources & evidence

ORD record
ord-9f33ce5de7f64bda89ddf3b2b500a09f
Source dataset
uspto-grants-1987_05
Patent number
US04668640

Reaction notes

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