Ethanol → HCID 178480057, 화합물

HRID 486112노트

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HRID 486112 반응식
[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]

참가 물질

6

실험 절차

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).

후처리

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

출처 및 근거

ORD 기록
ord-fca87508b6a64f1d9bae01926eb555c0
출처 데이터셋
uspto-grants-1994_03
특허 번호
US05290800

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