1,2-Dichloroethane → tert-Butyl 3-(1-Pivaloyl-1H-indazol-5-ylamino)piperidine-1-carboxylate

HRID 1911991노트

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HRID 1911991 반응식
O=[C:2]1[CH2:7][CH2:6][CH2:5][N:4]([C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9])[CH2:3]1.ClCCCl.C(O)(=O)/C=C\C(O)=O.[NH2:27][C:28]1[CH:29]=[C:30]2[C:34](=[CH:35][CH:36]=1)[N:33]([C:37](=[O:42])[C:38]([CH3:41])([CH3:40])[CH3:39])[N:32]=[CH:31]2.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>C(=O)(O)[O-].[Na+]>[C:37]([N:33]1[C:34]2[C:30](=[CH:29][C:28]([NH:27][CH:2]3[CH2:7][CH2:6][CH2:5][N:4]([C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9])[CH2:3]3)=[CH:36][CH:35]=2)[CH:31]=[N:32]1)(=[O:42])[C:38]([CH3:41])([CH3:40])[CH3:39]

참가 물질

6

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온도
20 °C

실험 절차

Into a 1 L 3-neck round bottom flask fitted with a nitrogen inlet and mechanical stirrer was added tert-butyl 3-oxopiperidine-1-carboxylate (14.2 g, 0.07 mol), 1,2-dichloroethane (300 mL), and 1-(5-amino-1H-indazol-1-yl)-2,2-dimethylpropan-1-one maleate salt (23.0 g, 0.07 mol). The vessel was purged with nitrogen and stirred at 20° C. for one hour. Sodium triacetoxyborohydride (19.0 g, 0.09 mol) was added, and the reaction was monitored by analytical TLC to completion. The reaction was diluted with 100 mL of saturated sodium bicarbonate. The organic phase was isolated, dried over MgSO4, filtered and evaporated to dryness to afford the title compound as a yellow solid (25.0 g, 91%).

후처리

  1. customInto a 1 L 3-neck round bottom flask fitted with a nitrogen inlet and mechanical stirrer
  2. customThe vessel was purged with nitrogen
  3. customThe organic phase was isolated
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. customevaporated to dryness

출처 및 근거

ORD 기록
ord-9fbb86af749941089a178d466d775f55
출처 데이터셋
uspto-grants-2013_12
특허 번호
US08604218B2

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