1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 1-[(15-methyl-8-nitrotetracyclo[6.6.2.02,7.09,14]hexadeca-2,4,6,9,11,13-hexaen-15-yl)carbonyl]-3-(1-naphthyl)-1H-1,2,4-triazol-5-amine

HRID 1988780ノート

反応式

HRID 1988780 の反応式
[CH3:1][C:2]1([C:21]([OH:23])=O)[CH2:17][C:10]2([N+:18]([O-:20])=[O:19])[C:11]3[C:16]([CH:3]1[C:4]1[C:9]2=[CH:8][CH:7]=[CH:6][CH:5]=1)=[CH:15][CH:14]=[CH:13][CH:12]=3.ON1C2C=CC=CC=2N=N1.C(N(C(C)C)C(C)C)C.CCN=C=NCCCN(C)C.[C:54]1([C:64]2[NH:68][N:67]=[C:66]([NH2:69])[N:65]=2)[C:63]2[C:58](=[CH:59][CH:60]=[CH:61][CH:62]=2)[CH:57]=[CH:56][CH:55]=1>C(#N)C>[CH3:1][C:2]1([C:21]([N:67]2[C:66]([NH2:69])=[N:65][C:64]([C:54]3[C:63]4[C:58](=[CH:59][CH:60]=[CH:61][CH:62]=4)[CH:57]=[CH:56][CH:55]=3)=[N:68]2)=[O:23])[CH2:17][C:10]2([N+:18]([O-:20])=[O:19])[C:11]3[C:16]([CH:3]1[C:4]1[C:9]2=[CH:8][CH:7]=[CH:6][CH:5]=1)=[CH:15][CH:14]=[CH:13][CH:12]=3

参加物

7

反応物 5

HCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 757711-HydroxybenzotriazoleHCID 81531DiisopropylethylamineHCID 36979375-(naphthalen-1-yl)-4H-1,2,4-triazol-3-amineHCID 596985749-Nitro-9,10-dihydro-11-methyl-9,10-ethanoanthracene-11-carboxylic acid

生成物 1

HCID 591273591-[(15-methyl-8-nitrotetracyclo[6.6.2.02,7.09,14]hexadeca-2,4,6,9,11,13-hexaen-15-yl)carbonyl]-3-(1-naphthyl)-1H-1,2,4-triazol-5-amine収率 94%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

To a stirred solution of 15-methyl-8-nitrotetracyclo[6.6.2.02,7.09,14]hexadeca-2,4,6,9,11,13-hexaene-15-carboxylic acid (22 mg, 0.07 mmol, prepared according to WO04009017), 1-hydroxybenzotriazole (14 mg, 0.11 mmol), and N-ethyl-N,N-diisopropylamine (0.25 mL) in anhydrous acetonitrile (2 mL) was added EDCI (34 mg, 0.18 mmol) at RT under argon. After the mixture was stirred at RT for 10 min, 5-(naphthalen-1-yl)-1H-1,2,4-triazol-3-amine (22 mg, 0.1 mmol) was added. The reaction mixture was stirred at RT overnight and at 80° C. for 1 h. After the solvents were removed, the residue was partitioned between methylene chloride and saturated aqueous sodium bicarbonate solution. The aqueous solution was extracted with methylene chloride. The combined organic solutions were dried (Na2SO4), concentrated and purified by silica gel chromatography to give 33 mg (94% yield) of the title compound as a white solid. (M+H)+=502.26.

後処理

  1. stirringThe reaction mixture was stirred at RT overnight and at 80° C. for 1 h
  2. customAfter the solvents were removed
  3. customthe residue was partitioned between methylene chloride and saturated aqueous sodium bicarbonate solution
  4. extractionThe aqueous solution was extracted with methylene chloride
  5. dry with materialThe combined organic solutions were dried (Na2SO4)
  6. concentrationconcentrated
  7. custompurified by silica gel chromatography

出典と根拠

ORDレコード
ord-53049c5906254763940fb452079eeaf4
出典データセット
uspto-grants-2010_01
特許番号
US07642273B2

反応ノート

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