Isopropyl chloroformate → 4-[4-(6-Cyano-2,3-difluoro-phenoxy)-pyrazolo-[3,4-d]pyrimidin-1-yl]-piperidine-1-carboxylic acid isopropyl ester

HRID 1931629ノート

反応式

HRID 1931629 の反応式
ClC(OC(C)C)=O.FC(F)(F)C(O)=O.FC1C(OC2N=CN=C3N(C4CCNCC4)N=CC=23)=C(C=CC=1F)C#N.[C:41]([O:45][C:46]([N:48]1[CH2:53][CH2:52][CH:51]([N:54]2[C:58]3=[N:59][CH:60]=[N:61][C:62]([O:63][C:64]4[C:69]([C:70]#[N:71])=[CH:68][CH:67]=[C:66]([F:72])[C:65]=4[F:73])=[C:57]3[CH:56]=[N:55]2)[CH2:50][CH2:49]1)=[O:47])(C)([CH3:43])[CH3:42].FC(F)(F)C(O)=O.C(OC1C=CC(OC2N=CN=C3N(C4CCNCC4)N=CC=23)=C(F)C=1)C.C(N(C(C)C)CC)(C)C>ClCCl.O>[CH:41]([O:45][C:46]([N:48]1[CH2:49][CH2:50][CH:51]([N:54]2[C:58]3=[N:59][CH:60]=[N:61][C:62]([O:63][C:64]4[C:69]([C:70]#[N:71])=[CH:68][CH:67]=[C:66]([F:72])[C:65]=4[F:73])=[C:57]3[CH:56]=[N:55]2)[CH2:52][CH2:53]1)=[O:47])([CH3:43])[CH3:42]

参加物

8

反応物 5

HCID 7917Isopropyl chloroformateHCID 81531DiisopropylethylamineHCID 579649274-[4-(6-Cyano-2,3-difluoro-phenoxy)-pyrazolo[3,4-d]pyrimidin-1-yl]-piperidine-1-carboxylic acid tert-butyl esterHCID 669153124-(4-ethoxy-2-fluoro-phenoxy)-1-piperidin-4-yl-1H-pyrazolo[3,4-d]pyrimidine trifluoroacetate saltHCID 690162343,4-difluoro-2-(1-piperidin-4-yl-1H-pyrazolo[3,4-d]pyrimidine-4-yloxy)-benzonitrile trifluoroacetate salt

生成物 1

HCID 579649534-[4-(6-Cyano-2,3-difluoro-phenoxy)-pyrazolo-[3,4-d]pyrimidin-1-yl]-piperidine-1-carboxylic acid isopropyl ester収率 85%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6344Dichloromethane溶媒

実験手順

Isopropyl chloroformate (Aldrich Chemical Company, Inc., Milwaukee, Wis., USA 1M in toluene; 0.35 mL, 0.35 mmol) was added to a mixture of 3,4-difluoro-2-(1-piperidin-4-yl-1H-pyrazolo[3,4-d]pyrimidine-4-yloxy)-benzonitrile trifluoroacetate salt (which was prepared from 4-[4-(6-cyano-2,3-difluoro-phenoxy)-pyrazolo[3,4-d]pyrimidin-1-yl]-piperidine-1-carboxylic acid tert-butyl ester [Example 49] following the procedure described for the preparation of Intermediate 29; 180 mg, 0.35 mmol), diisopropylethylamine (136 mg, 1.06 mmol) in dichloromethane (6 mL). The reaction was stirred at room temperature overnight. Water was added to quench the reaction and the aqueous layer was extracted three times with dichloromethane. The combined organic layers were dried (sodium sulfate), filtered, evaporated and purified by flash chromatography on silica gel, eluting with 4% methanol/dichloromethane to give 4-[4-(6-cyano-2,3-difluoro-phenoxy)-pyrazolo-[3,4-d]pyrimidin-1-yl]-piperidine-1-carboxylic acid isopropyl ester (147 mg, 85%) as a white solid. Mass spectrum MH+=443.

後処理

  1. customto quench
  2. customthe reaction
  3. extractionthe aqueous layer was extracted three times with dichloromethane
  4. dry with materialThe combined organic layers were dried (sodium sulfate)
  5. filtrationfiltered
  6. customevaporated
  7. custompurified by flash chromatography on silica gel
  8. washeluting with 4% methanol/dichloromethane

出典と根拠

ORDレコード
ord-948ea6ec3e0e4e2cbd2967d533652021
出典データセット
uspto-grants-2012_05
特許番号
US08188098B2

反応ノート

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