Ethanol → HCID 178480057、化合物

HRID 486112ノート

反応式

HRID 486112 の反応式
[CH3:1][C:2]([C:5]1[CH:6]=[C:7]([CH:16]=[C:17]2[N:21]([CH3:22])[C:20](SC)=[N:19][C:18]2=[O:25])[CH:8]=[C:9]([C:12]([CH3:15])([CH3:14])[CH3:13])[C:10]=1[OH:11])([CH3:4])[CH3:3].Cl.[NH2:27][C:28]([NH2:30])=[NH:29].C(O)C.CC(C)([O-])C.[K+]>O>[CH3:1][C:2]([C:5]1[CH:6]=[C:7]([CH:16]=[C:17]2[N:21]([CH3:22])[C:20]([NH:29][C:28]([NH2:30])=[NH:27])=[N:19][C:18]2=[O:25])[CH:8]=[C:9]([C:12]([CH3:15])([CH3:14])[CH3:13])[C:10]=1[OH:11])([CH3:4])[CH3:3]

参加物

6

実験手順

A mixture of 5-[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]methylene]-1,5-dihydro-1-methyl-2-(methylthio)-4H-imidazol-4-one (3.0 g, 8 mmoles), guanidine hydrochloride (1.7 g, 18 mmoles) and 50 mL of ethanol is treated with potassium t-butoxide (1.5 g, 13 mmoles) and heated under reflux for 20 hours, then stirred into 400 mL of water. The precipitate is filtered off, rinsed with water, dried, and recrystallized from acetone to afford the product (1.4 g), mp 286°-287° C. (dec). A sample recrystallized from DMF/EtOH was analytically pure which is N-[5-[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]methylene]-4,5-dihydro-1-methyl-4-oxo-1H-imidazol-2-yl]guanidine, mp 288°-290° C. (dec).

後処理

  1. temperatureheated
  2. temperatureunder reflux for 20 hours
  3. filtrationThe precipitate is filtered off
  4. washrinsed with water
  5. customdried
  6. customrecrystallized from acetone

出典と根拠

ORDレコード
ord-fca87508b6a64f1d9bae01926eb555c0
出典データセット
uspto-grants-1994_03
特許番号
US05290800

反応ノート

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