Triethylamine → tert-Butyl 4-{[2-(ethoxyacetyl)hydrazino]carbonyl}piperidine-1-carboxylate

HRID 419850

反応式

HRID 419850 の反応式
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH:11]([C:14]([NH:16][NH2:17])=[O:15])[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH2:18]([O:20][CH2:21][C:22](O)=[O:23])[CH3:19].Cl.CN(C)CCCN=C=NCC.O.ON1C2C=CC=CC=2N=N1.C(N(CC)CC)C>CN(C)C=O>[CH2:18]([O:20][CH2:21][C:22]([NH:17][NH:16][C:14]([CH:11]1[CH2:12][CH2:13][N:8]([C:6]([O:5][C:1]([CH3:4])([CH3:2])[CH3:3])=[O:7])[CH2:9][CH2:10]1)=[O:15])=[O:23])[CH3:19]

参加物

7

実験手順

A mixture of 4-hydrazinocarbonyl-piperidine-1-carboxylic acid tert-butyl ester (WO 2000039125, prep 27) (3 g, 12.33 mmol), ethoxyacetic acid (1.28 mL, 13.56 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (2.6 g, 13.56 mmol), 1-hydroxybenzotriazole hydrate (1.83 g, 13.56 mmol) and triethylamine (2.1 mL, 14.8 mmol) in N,N-dimethylformamide (15 mL) was stirred at room temperature for 18 hours. The mixture was concentrated under reduced pressure and the residue was partitioned between ethyl acetate and aqueous sodium carbonate solution. The layers were separated, the organic phase was dried over MgSO4 and evaporated under reduced pressure to provide the title compound as an oil, that crystallised on standing.

後処理

  1. concentrationThe mixture was concentrated under reduced pressure
  2. customthe residue was partitioned between ethyl acetate and aqueous sodium carbonate solution
  3. customThe layers were separated
  4. dry with materialthe organic phase was dried over MgSO4
  5. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-550260baae444d04aaa2bb4b4d2ba678
出典データセット
uspto-grants-2012_01
特許番号
US08093400B2

関連ノート

読み込み中…