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Diisopropylethylamine → tert-butyl N-[N-(5-propan-2-yl-1-quinolin-6-ylpyrazole-4-carbonyl)carbamimidoyl]carbamate

HRID 488805
ノート
印刷プレビュー

反応式

HRID 488805 の反応式
[CH:1]([C:4]1[N:8]([C:9]2[CH:10]=[C:11]3[C:16](=[CH:17][CH:18]=2)[N:15]=[CH:14][CH:13]=[CH:12]3)[N:7]=[CH:6][C:5]=1[C:19](O)=[O:20])([CH3:3])[CH3:2].C(N(CC)C(C)C)(C)C.F[P-](F)(F)(F)(F)F.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1.[C:58]([O:62][C:63]([NH:65][C:66]([NH2:68])=[NH:67])=[O:64])([CH3:61])([CH3:60])[CH3:59]>CN(C)C=O>[C:58]([O:62][C:63]([NH:65][C:66]([NH:68][C:19]([C:5]1[CH:6]=[N:7][N:8]([C:9]2[CH:10]=[C:11]3[C:16](=[CH:17][CH:18]=2)[N:15]=[CH:14][CH:13]=[CH:12]3)[C:4]=1[CH:1]([CH3:2])[CH3:3])=[O:20])=[NH:67])=[O:64])([CH3:61])([CH3:59])[CH3:60]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 81531DiisopropylethylamineHCID 151348Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 222676405-isopropyl-1-(6-quinolinyl)-1H-pyrazole-4-carboxylic acidHCID 178454308HCID 178454308、化合物

生成物 1

HCID 141011648tert-butyl N-[N-(5-propan-2-yl-1-quinolin-6-ylpyrazole-4-carbonyl)carbamimidoyl]carbamate収率 22.5%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a solution of 5-isopropyl-1-(6-quinolinyl)-1H-pyrazole-4-carboxylic acid (336.7 mg, 1.2 mmol) in 5 ml dimethylformamide was added N,N-diisopropylethylamine (0.42 ml, 2.39 mmol), benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate (BOP reagent) (582 mg, 1.32 mmol) and tert-butoxycarbonylguanidine (210 mg, 1.32 mmol). The resulting solution was stirred at room temperature for 2 h, then heated to 60° C. for 2 h. The reaction mixture was then cooled to room temperature and concentrated to dryness in vacuo. The solid residue was partitioned between ethyl acetate and water. The ethyl acetate layer was washed with brine, dried (sodium sulfate) and concentrated to dryness in vacuo. The solid residue was triturated with methanol (1.5 ml), filtered, washed with diethyl ether and dried to yield the title compound as a white solid (114.3 mg, 22.5% yield).

後処理

  1. temperatureheated to 60° C. for 2 h
  2. temperatureThe reaction mixture was then cooled to room temperature
  3. concentrationconcentrated to dryness in vacuo
  4. customThe solid residue was partitioned between ethyl acetate and water
  5. washThe ethyl acetate layer was washed with brine
  6. dry with materialdried (sodium sulfate)
  7. concentrationconcentrated to dryness in vacuo
  8. customThe solid residue was triturated with methanol (1.5 ml)
  9. filtrationfiltered
  10. washwashed with diethyl ether
  11. customdried

出典と根拠

ORDレコード
ord-9fcc380d12e54b589c47d7110a0a176e
出典データセット
uspto-grants-2005_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06974813B2

反応ノート

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