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HCID 135525218、化合物 → N-methyl-2-(2-hydroxyphenyl)-2-methoxyiminoacetamide

HRID 432058
ノート
印刷プレビュー

反応式

HRID 432058 の反応式
[CH3:1][NH:2][C:3](=[O:15])/[C:4](/[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[OH:14])=[N:5]/[O:6][CH3:7].CNC(=O)/C(/C1C=CC=CC=1O)=N\OC>>[CH3:1][NH:2][C:3](=[O:15])[C:4]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[OH:14])=[N:5][O:6][CH3:7]
参加物実験手順出典と根拠反応ノート

参加物

3

反応物 2

HCID 135525218HCID 135525218、化合物HCID 135532297HCID 135532297、化合物

生成物 1

HCID 136045378N-methyl-2-(2-hydroxyphenyl)-2-methoxyiminoacetamide

実験手順

9.68 g of crude product (0.0339 mol of methyl E/Z-2-(2-hydroxyphenyl)-2-methoxyimino-acetate, in particular compound II-1c from process step 6, HPLC: 43.7% E isomer of log p=1.48; 29.4% Z isomer of log p=2.37) are dissolved in 100 ml of tetrahydrofuran and cooled to 10° C. With cooling, methylamine is introduced. After about 30 minutes, 50 ml of methanol are added, the solution is saturated with methylamine and the mixture is allowed to stand at 10° C. overnight. The solvents are distilled off under reduced pressure and the residue is mixed with a mixture of 30 ml of 2N hydrochloric acid and 30 ml of saturated sodium chloride solution and extracted three times with 50 ml of ethyl acetate each time. The organic phase is dried over sodium sulphate and the solvent is distilled off under reduced pressure, giving 8.5 g of crude product which, according to HPLC, contains 52.6% N-methyl-E-2-(2-hydroxyphenyl)-2-methoxyimino-acetamide of log p=0.98 and 31.9% N-methyl-Z-2-(2-hydroxyphenyl)-2-methoxyiminoacetamide of log p=1.29.

出典と根拠

ORDレコード
ord-20d74a9b4461417b920804ea07d1caa9
出典データセット
uspto-grants-2003_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06660872B1

反応ノート

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