Pivaloyl chloride → Ethyl 5-(2,2-dimethylpropanoyl)-3-[(4-fluorobenzoyl)amino]-6,6-dimethyl-5,6-dihydropyrrolo[3,4-c]pyrazole-1(4H)-carboxylate

HRID 1042384ノート

反応式

HRID 1042384 の反応式
Cl.[F:2][C:3]1[CH:26]=[CH:25][C:6]([C:7]([NH:9][C:10]2[C:11]3[CH2:22][NH:21][C:20]([CH3:24])([CH3:23])[C:12]=3[N:13]([C:15]([O:17][CH2:18][CH3:19])=[O:16])[N:14]=2)=[O:8])=[CH:5][CH:4]=1.C(N(CC)C(C)C)(C)C.[C:36](Cl)(=[O:41])[C:37]([CH3:40])([CH3:39])[CH3:38].CCOC(C)=O.CCCCCC>ClCCl>[CH3:38][C:37]([CH3:40])([CH3:39])[C:36]([N:21]1[CH2:22][C:11]2[C:10]([NH:9][C:7](=[O:8])[C:6]3[CH:5]=[CH:4][C:3]([F:2])=[CH:26][CH:25]=3)=[N:14][N:13]([C:15]([O:17][CH2:18][CH3:19])=[O:16])[C:12]=2[C:20]1([CH3:23])[CH3:24])=[O:41]

参加物

6

実験手順

Ethyl 3-[(4-fluorobenzoyl)amino]-6,6-dimethyl-5,6-dihydropyrrolo[3,4-c]pyrazole-1(4H)-carboxylate hydrochloride (2.0 g, 5.77 mmol) in dichloromethane (70 ml) was treated, at 0° C., with N,N-diisopropylethylamine (1.6 ml, 9.2 mmol, 1.6 eq) and with pivaloyl chloride (780 μL, 6.3 mmol, 1.1 eq). Gradually, the reaction was brought to room temperature and stirred overnight (TLC: CH2Cl2/EtOAc 90/10). The solution was washed with saturated sodium hydrogencarbonate aqueous solution and brine. The organic phase was dried over sodium sulfate, evaporated and purified by flash chromatography (eluent: CH2Cl2/EtOAc 90/10) to afford 2.03 g of the title compound in 82% yield.

後処理

  1. customwas brought to room temperature
  2. washThe solution was washed with saturated sodium hydrogencarbonate aqueous solution and brine
  3. dry with materialThe organic phase was dried over sodium sulfate
  4. customevaporated
  5. custompurified by flash chromatography (eluent: CH2Cl2/EtOAc 90/10)

出典と根拠

ORDレコード
ord-2d05e6d64d684f82b85e5442121cf10f
出典データセット
uspto-grants-2013_10
特許番号
US08557845B2

反応ノート

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