Triethylamine → 1-((8-(2-Ethyl-6-methylbenzylamino)-2,3-dimethylimidazo[1,2-a]pyridin-6-yl)carbonyl)-2-(s)-pyrrolidinecarboxamide

HRID 427476

反応式

HRID 427476 の反応式
[CH3:1][C:2]1[N:3]=[C:4]2[C:9]([NH:10][CH2:11][C:12]3[C:17]([CH3:18])=[CH:16][CH:15]=[CH:14][C:13]=3[CH2:19][CH3:20])=[CH:8][C:7]([C:21](O)=[O:22])=[CH:6][N:5]2[C:24]=1[CH3:25].[B-](F)(F)(F)F.CN(C(ON1N=NC2C1=CC=CC=2)=[N+](C)C)C.C(N(CC)CC)C.[NH:55]1[CH2:62][CH2:61][CH2:60][C@H:56]1[C:57]([NH2:59])=[O:58]>C(Cl)Cl>[CH2:19]([C:13]1[CH:14]=[CH:15][CH:16]=[C:17]([CH3:18])[C:12]=1[CH2:11][NH:10][C:9]1[C:4]2[N:5]([C:24]([CH3:25])=[C:2]([CH3:1])[N:3]=2)[CH:6]=[C:7]([C:21]([N:55]2[CH2:62][CH2:61][CH2:60][C@H:56]2[C:57]([NH2:59])=[O:58])=[O:22])[CH:8]=1)[CH3:20]

参加物

6

実験手順

2,3-dimethyl-8-(2-ethyl-6-methylbenzylamino)-imidazo[1,2-a]pyridine-6-carboxylic acid (0.15 g, 0.44 mmol), o-Benzotriazol-1-yl-N,N,N′,N′-Tetramethyluronium tetrafluoroborate (TBTU)(0.14 g, 0.45 mmol) and triethylamine (0.05 g, 0.5 mmol) were added to methylene chloride (10 ml) and the mixture was stirred for 10 min. (S)-prolinamide (0.016 g, 0.45 mmol) was added and the reaction mixture was stirred at ambient temperature for 1 h. The solvent was evaporated under reduced pressure and purification of the residue by column chromatography on silica gel using methylene chloride:methanol (9:1) as eluent and crystallization from diethyl ether gave 0.07 g (36%) of the title compound.

後処理

  1. additionwas added
  2. customThe solvent was evaporated under reduced pressure and purification of the residue by column chromatography on silica gel
  3. customcrystallization from diethyl ether

出典と根拠

ORDレコード
ord-0e78413df04e46e3ad2bd563c26aa502
出典データセット
uspto-grants-2001_11
特許番号
US06313136B1

関連ノート

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