Diazomethane → HCID 14995415, compound

HRID 2379605Notes

Reaction equation

HRID 2379605 reaction equation
[CH:1]1[C:10]2[C:5](=[C:6]([NH:11][C:12](=[O:35])[CH:13]([CH2:31][C:32]([OH:34])=[O:33])[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])[CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][N:2]=1.[N+](=[CH2:38])=[N-]>CCOCC>[CH:1]1[C:10]2[C:5](=[C:6]([NH:11][C:12](=[O:35])[CH:13]([CH2:31][C:32]([O:34][CH3:38])=[O:33])[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])[CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][N:2]=1

Participants

4

Reactant 2

HCID 9550DiazomethaneHCID 14995414HCID 14995414, compound

Product 1

HCID 14995415HCID 14995415, compound

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent

Procedure

Commercially available N-(isoquinolin-5-yl )-2-(carboxymethyl)nonadecanoic amide was esterified with diazomethane in ether to give the title compound.

Sources & evidence

ORD record
ord-d38680f933dd4693a8f2e5c4f63e7c58
Source dataset
uspto-grants-1994_11
Patent number
US05362878

Reaction notes

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