Oxalyl chloride → HCID 56640442, compound

HRID 1186742Notes

Reaction equation

HRID 1186742 reaction equation
[NH2:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[CH:4][C:3]=1[NH:12][C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([C:19]2[O:23][N:22]=[C:21]([CH3:24])[N:20]=2)[CH:14]=1.[C:25](Cl)(=[O:29])[C:26](Cl)=[O:27]>>[CH3:24][C:21]1[N:20]=[C:19]([C:15]2[CH:14]=[C:13]([N:12]3[C:3]4[CH:4]=[CH:5][C:6]5[CH:7]=[CH:8][CH:9]=[CH:10][C:11]=5[C:2]=4[NH:1][C:26](=[O:27])[C:25]3=[O:29])[CH:18]=[CH:17][CH:16]=2)[O:23][N:22]=1

Participants

3

Reactant 2

HCID 65578Oxalyl chlorideHCID 86690014HCID 86690014, compound

Product 1

HCID 56640442HCID 56640442, compound

Procedure

1-Amino-2-[3-(3-methyl-[1,2,4]oxadiazol-5-yl)phenyl]aminonaphthalene and oxalyl chloride were used in a process similar to Example 1(3) to give the titled compound.

Sources & evidence

ORD record
ord-f9a23d1aca3c41fa8e34dfe402316d0e
Source dataset
uspto-grants-2014_03
Patent number
US08673915B2

Reaction notes

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