Pyridine → HCID 67248809、化合物

HRID 1035320ノート

反応式

HRID 1035320 の反応式
[C:1]([O:5][C:6]([NH:8][C@H:9]([CH2:13][C:14]([O:16][CH3:17])=[O:15])[C:10]([OH:12])=O)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH2:18]([O:20][C:21](=[O:31])[CH2:22][NH:23][CH2:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)[CH3:19].Cl.CN(C)CCCN=C=NCC.N1C=CC=CC=1>ClCCl>[CH2:24]([N:23]([CH2:22][C:21]([O:20][CH2:18][CH3:19])=[O:31])[C:10](=[O:12])[C@H:9]([NH:8][C:6]([O:5][C:1]([CH3:2])([CH3:3])[CH3:4])=[O:7])[CH2:13][C:14]([O:16][CH3:17])=[O:15])[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1

参加物

6

実験手順

To a solution of Example 255B (31.28 g, 126.6 mmol) in dichloromethane (500 mL) was added N-benzylglycine ethyl ester (24.46 g, 126.6 mol), N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (24.3 g, 126.6 mmol), and pyridine (70 mL). After addition of the reagents, the reaction was allowed to warm to ambient temperature and stirred for 16 hours. The solution was concentrated and then partitioned between ethyl acetate and HCl (1 M, aqueous). The organic solvent was collected, and the aqueous again washed with ethyl acetate. The organic solvent was combined, washed with K2CO3 (2 M aqueous), washed with brine, and dried with MgSO4. Concentration of the dried solution afforded the title compound.

後処理

  1. additionAfter addition of the reagents
  2. concentrationThe solution was concentrated
  3. custompartitioned between ethyl acetate and HCl (1 M, aqueous)
  4. customThe organic solvent was collected
  5. washthe aqueous again washed with ethyl acetate
  6. washwashed with K2CO3 (2 M aqueous)
  7. washwashed with brine
  8. dry with materialdried with MgSO4

出典と根拠

ORDレコード
ord-994122d4b9b843f28fd6fe5f87f6a6ac
出典データセット
uspto-grants-2013_10
特許番号
US08546377B2

反応ノート

読み込み中…