Triethylamine → HCID 86590086, compound

HRID 2216425Notes

Reaction equation

HRID 2216425 reaction equation
[O:1]1[C:5]([C:6]([OH:8])=O)=[CH:4][C:3]2[CH:9]=[CH:10][CH:11]=[CH:12][C:2]1=2.Cl.N[C:15]1[CH:16]=[CH:17][C:18]([O:23][CH2:24][C:25]([CH3:29])([CH3:28])[CH2:26][OH:27])=[C:19]([CH:22]=1)[C:20]#[N:21].C([N:32](CC)CC)C>>[C:20]([C:19]1[CH:22]=[C:15]([C:4]2[C:3]3[CH:9]=[CH:10][CH:11]=[CH:12][C:2]=3[O:1][C:5]=2[C:6]([NH2:32])=[O:8])[CH:16]=[CH:17][C:18]=1[O:23][CH2:24][C:25]([CH3:28])([CH3:29])[CH2:26][OH:27])#[N:21]

Participants

4

Reactant 3

HCID 8471TriethylamineHCID 10331Benzofuran-2-carboxylic acidHCID 219423175-Amino-2-(2,2-dimethyl-3-hydroxypropoxy)benzonitrile monohydrochloride

Product 1

HCID 86590086HCID 86590086, compound

Procedure

By the reaction and treatment in the same manner as in Example 6 using benzo[b]furan-2-carboxylic acid (0.7 g), 5-amino-2-(2,2-dimethyl-3-hydroxypropoxy)benzonitrile monohydrochloride (1.0 g) and triethylamine (0.6 ml), the title compound (0.26 g) was obtained. melting point: 199-201° C.

Sources & evidence

ORD record
ord-303cbd8d013844e89f7a6cfa3f83c3b9
Source dataset
uspto-grants-2006_09
Patent number
US07112594B2

Reaction notes

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