1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → Ethyl 3-(5-{5-[3-chloro-4-(ethyloxy)phenyl]-1,2,4-oxadiazol-3-yl}-1H-indazol-1-yl)propanoate

HRID 2189783ノート

反応式

HRID 2189783 の反応式
[OH:1][NH:2][C:3](=[NH:20])[C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[N:9]([CH2:13][CH2:14][C:15]([O:17][CH2:18][CH3:19])=[O:16])[N:8]=[CH:7]2.[Cl:21][C:22]1[CH:23]=[C:24]([CH:28]=[CH:29][C:30]=1[O:31][CH2:32][CH3:33])[C:25](O)=O.CCN=C=NCCCN(C)C.C1C=CC2N(O)N=NC=2C=1>CN(C=O)C>[Cl:21][C:22]1[CH:23]=[C:24]([C:25]2[O:1][N:2]=[C:3]([C:4]3[CH:5]=[C:6]4[C:10](=[CH:11][CH:12]=3)[N:9]([CH2:13][CH2:14][C:15]([O:17][CH2:18][CH3:19])=[O:16])[N:8]=[CH:7]4)[N:20]=2)[CH:28]=[CH:29][C:30]=1[O:31][CH2:32][CH3:33]

参加物

6

実験手順

Ethyl 3-{5-[(hydroxyamino)(imino)methyl]-1H-indazol-1-yl}propanoate (D52) (265 mg, 0.96 mmol) and 3-Chloro-4-(ethyloxy)benzoic acid (D7) (192 mg, 0.96 mmol) were stirred together in DMF (5 ml) at 80° C. and EDAC (203 mg) and HOBt (142 mg) were added. When the reaction was judged to be complete (analysis by LCMS) it was cooled and the reaction mixture was partitioned between EtOAc and aq. sodium bicarbonate solution. The organic layer was separated and washed with water, dried and evaporated and triturated with ethanol to give the crude product. Purification by flash chromatography (EtOAc/hexane 1:3 to 1:1) to afforded the title compound (87 mg) as a white solid. MS (ES): C22H2135ClN4O4 requires 440 found (MH+) 441.

後処理

  1. temperaturewas cooled
  2. customthe reaction mixture was partitioned between EtOAc and aq. sodium bicarbonate solution
  3. customThe organic layer was separated
  4. washwashed with water
  5. customdried
  6. customevaporated
  7. customtriturated with ethanol
  8. customto give the crude product
  9. customPurification by flash chromatography (EtOAc/hexane 1:3 to 1:1)

出典と根拠

ORDレコード
ord-1e15310189534547a73f910fa1a3b681
出典データセット
uspto-grants-2012_12
特許番号
US08324254B2

反応ノート

読み込み中…