Formaldehyde → 1-Hydroxymethyl-3,5-dimethyl-1,2,4-triazole

HRID 614702

反応式

HRID 614702 の反応式
[CH3:1][C:2]1[N:6]=[C:5]([CH3:7])[NH:4][N:3]=1.C=O.S(Cl)(Cl)=O.ClCN1C(C)=NC(C)=N1.[OH:23][C:24]1C2C(=CC=CC=2)C(O)=CC=1C(NCCCOC1C=CC(C(CC)(C)C)=CC=1C(CC)(C)C)=O.[O-]CC.[Na+]>CN(C=O)C>[OH:23][CH2:24][N:3]1[C:2]([CH3:1])=[N:6][C:5]([CH3:7])=[N:4]1

参加物

8

実験手順

1-Hydroxymethyl-3,5-dimethyl-1,2,4-triazole which was prepared from 3,5-dimethyl-1,2,4-triazole and formaldehyde was reacted with 1.5 to 5 times on a molar basis of thionyl chloride to prepare 1-chloromethyl-3,5-dimethyl-1,2,4-triazole. This was reacted with an equimolar amount of 1,4-dihydroxy-N-[γ-(2,4-di-tert-amylphenoxy)propyl]-2-naphthamide in DMF in the presence of 1.5 to 3 times on a molar basis of sodium ethoxide to obtain Coupler (36).

出典と根拠

ORDレコード
ord-1e4157c148b84269a4fe0c5d445ebf7d
出典データセット
uspto-grants-1979_03
特許番号
US04146396

関連ノート

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