Benzaldehyde → HCID 178419071, compound

HRID 7517

Reaction equation

HRID 7517 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1.[C:8]([N+:12]#[C-:13])([CH3:11])([CH3:10])[CH3:9].[CH:14](=O)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.[CH2:22]([C:29]([Cl:31])=[O:30])[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27]C>Cl(O)(=O)(=O)=O>[Cl-:31].[C:8]([N:12]([C:29](=[O:30])[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])[C:13]1[N:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]2=[N+:1]([C:29](=[O:30])[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])[C:14]=1[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)([CH3:11])([CH3:10])[CH3:9]

Participants

6

Reactant 4

HCID 240BenzaldehydeHCID 8124Octanoyl chlorideHCID 104392-AminopyridineHCID 23577Tert-Butyl isocyanide

Product 1

HCID 178419071HCID 178419071, compound

Reagents, catalysts & solvents 1

HCID 24247Perchloric AcidSolvent

Procedure

Example 11 was carried out in accordance with the general directions for synthesis in process step a) from 1.0 ml (0.1 mmol) 2-amino-pyridine (0.1 M, DCM), 0.575 ml (0.115 mmol) tert.-butylisonitrile solution (0.2 M, DCM), 0.500 ml (0.15 mmol) benzaldehyde solution (0.3 M, DCM) and 10 μl perchloric acid (w=20%) and in process steps b) to d) by reacting the resultant reaction product with 0.4 mmol heptylcarboxylic acid chloride.

Sources & evidence

ORD record
ord-fed35cec3dc043e3b9de4b02712093a2
Source dataset
uspto-grants-2006_08
Patent number
US07087607B2

Linked notes

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