Water → methyl-4-[(2-butyl-5-formyl-4-iodo-1H-imidazol-1-yl)methyl]naphthalene-1-carboxylate

HRID 37005노트

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HRID 37005 반응식
C(=O)([O-])[O-].[K+].[K+].[CH2:7]([C:11]1[NH:12][C:13]([CH:17]=[O:18])=[C:14]([I:16])[N:15]=1)[CH2:8][CH2:9][CH3:10].Br[CH2:20][C:21]1[C:30]2[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=2)[C:24]([C:31]([O:33][CH3:34])=[O:32])=[CH:23][CH:22]=1.O>CN(C)C=O>[CH3:34][O:33][C:31]([C:24]1[C:25]2[C:30](=[CH:29][CH:28]=[CH:27][CH:26]=2)[C:21]([CH2:20][N:12]2[C:13]([CH:17]=[O:18])=[C:14]([I:16])[N:15]=[C:11]2[CH2:7][CH2:8][CH2:9][CH3:10])=[CH:22][CH:23]=1)=[O:32]

참가 물질

6

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온도
70 °C

실험 절차

A suspension of 29.53 g (0.214 mol) of powdered potassium carbonate, 60.00 g (0.214 mol) of 2-butyl-4-iodoimidazole-5-carboxaldehyde and 65.68 g (0.235 mol) of methyl 4-bromomethylnaphthalene-1-carboxylate (E. A. Dixon, A. Fischer, and F. P. Robinson, Can. J. Chem, 59, 2629 (1981)) in 600 mL of dimethylformamide was stirred for 5 hours under argon at 70° C. An additional 6.56 g (0.0235 mol) of the bromomethyl ester was added and the suspension was stirred an additional 15 hours at 70° C. The reaction mixture was poured into water and the resulting solid was collected by filtration, washed with water, and triturated several times with 250 mL of boiling methanol to give 86.8 g (85%) of a solid; mp 177.5°-179° C.

후처리

  1. filtrationthe resulting solid was collected by filtration
  2. washwashed with water
  3. customtriturated several times with 250 mL of boiling methanol

출처 및 근거

ORD 기록
ord-0e22b46910f04957864882e451c7cb7c
출처 데이터셋
uspto-grants-1995_05
특허 번호
US05418250

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