2-Aminothiazole → HCID 22335556, compound

HRID 586568Notes

Reaction equation

HRID 586568 reaction equation
[NH2:1][C:2]1[S:3][CH:4]=[CH:5][N:6]=1.[C:7]([N+:11]#[C-:12])([CH3:10])([CH3:9])[CH3:8].[N:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[CH:19]=O>Cl(O)(=O)(=O)=O>[C:7]([NH:11][C:12]1[N:6]2[C:2]([S:3][CH:4]=[CH:5]2)=[N:1][C:19]=1[C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][N:13]=1)([CH3:10])([CH3:9])[CH3:8]

Participants

5

Reactant 3

HCID 21552-AminothiazoleHCID 142732-PyridinecarboxaldehydeHCID 23577Tert-Butyl isocyanide

Product 1

HCID 22335556HCID 22335556, compound

Reagents, catalysts & solvents 1

HCID 24247Perchloric AcidSolvent

Procedure

Compound 5 was prepared in accordance with the general synthesis instructions from 1.0 ml (0.1 mmol) 2-aminothiazole solution (0.1 M, MC), 0.575 ml (0.115 mmol) tert-butylisonitrile solution (0.2 M, MC), 0.500 ml (0.15 mmol) 2-pyridinecarbaldehyde solution (0.3 M, MC) and 10 μl perchloric acid (w=20%) in a substance library.

Sources & evidence

ORD record
ord-cdba70f023344cd5b92d25b0726df93e
Source dataset
uspto-grants-2005_08
Patent number
US06936631B2

Reaction notes

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