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Triethylamine → N-methyl-N-hydroxy-4-(3-(2-benzyloxyphenyl)propyl)benzamide

HRID 2395043
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HRID 2395043 반응식
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[CH2:15][CH2:16][CH2:17][C:18]1[CH:26]=[CH:25][C:21]([C:22](O)=[O:23])=[CH:20][CH:19]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C1CCC(N=C=NC2CCCCC2)CC1.Cl.[CH3:43][NH:44][OH:45].CCN(CC)CC>CN(C=O)C.C(Cl)Cl>[CH3:43][N:44]([OH:45])[C:22](=[O:23])[C:21]1[CH:25]=[CH:26][C:18]([CH2:17][CH2:16][CH2:15][C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=2[O:8][CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[CH:19][CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 8471TriethylamineHCID 10868DicyclohexylcarbodiimideHCID 77906N-methylhydroxylamine hydrochlorideHCID 189737644-(3-(2-Benzyloxyphenyl)propyl]benzoic acid

생성물 1

HCID 18973882N-methyl-N-hydroxy-4-(3-(2-benzyloxyphenyl)propyl)benzamide수율 36.1%

시약·촉매·용매 2

HCID 6228
Dimethylformamide
용매
HCID 6344Dichloromethane용매

실험 절차

A mixture of 4-(3-(2-benzyloxyphenyl)propyl]benzoic acid (1.0 g), 1-HOBT (0.39 g) and DCCI (0.595 g) in DMF (10 ml) was stirred for 3 hours, then added to a solution of N-methylhydroxylamine HCl (0.24 g) and Et3N (0.29 g) in CH2Cl2 (10 ml) and stirred for 70 hours. The product was extracted in 2N aqueous KOH and washed with ethyl acetate. The aqueous solution was acidified with concentrated HCl and extracted with diethyl ether. The solvent was evaporated and the residue subjected to flash chromatography on silica gel (using diethyl ether:methanol (95:5) as eluant) to give N-methyl-N-hydroxy-4-(3-(2-benzyloxyphenyl)propyl)benzamide as a gum (0.39 g).

후처리

  1. stirringstirred for 70 hours
  2. extractionThe product was extracted in 2N aqueous KOH
  3. washwashed with ethyl acetate
  4. extractionextracted with diethyl ether
  5. customThe solvent was evaporated

출처 및 근거

ORD 기록
ord-5bfdfe74464e4b01b0b7df5c5b5d7ece
출처 데이터셋
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05811459

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