1-Hydroxybenzotriazole → HCID 44124031、化合物
反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([CH:8]=[C:9]([C:11]([OH:13])=O)[N:10]=2)[CH:7]=1.Cl.CN(C)CCCN=C=NCC.ON1C2C=CC=CC=2N=N1.Cl.[CH3:37][NH:38][O:39][CH3:40]>ClCCl.O.C(N(CC)CC)C>[CH3:40][O:39][N:38]([CH3:37])[C:11]([C:9]1[N:10]=[C:5]2[CH:4]=[CH:3][C:2]([Cl:1])=[CH:7][N:6]2[CH:8]=1)=[O:13]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 3
実験手順
To a solution of 0.784 g of 6-chloroimidazo[1,2-a]pyridine-2-carboxylic acid in 12 mL of dichloromethane are added 1.67 mL of triethylamine, 1.53 g of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride and 1.08 g of 1-hydroxybenzotriazole. The reaction mixture is stirred for 20 minutes at room temperature. 0.39 g of N,O-dimethylhydroxylamine hydrochloride is added. The reaction mixture is stirred for 4 hours at room temperature. 60 mL of dichloromethane and 30 mL of water are added. After separation of the phases by settling, the organic phase is dried over magnesium sulfate, filtered, evaporated to dryness under reduced pressure, and then purified on a column of silica, eluting with a 95/5 mixture by volume of dichloromethane and methanol. The fractions containing the product are combined and concentrated to dryness under reduced pressure to give 0.6 g of N-methoxy-N-methyl-6-chloroimidazo[1,2-a]pyridine-2-carboxamide in the form of a white solid.
後処理
- stirringThe reaction mixture is stirred for 4 hours at room temperature
- customAfter separation of the phases
- dry with materialthe organic phase is dried over magnesium sulfate
- filtrationfiltered
- customevaporated to dryness under reduced pressure
- custompurified on a column of silica
- washeluting with a 95/5 mixture by volume of dichloromethane and methanol
- additionThe fractions containing the product
- concentrationconcentrated to dryness under reduced pressure
出典と根拠
- ORDレコード
- ord-b0b6798e70964e929fc875a3d4a92655
- 出典データセット
- uspto-grants-2011_03
- 特許番号
- US07902219B2
反応ノート
読み込み中…