4-Methylmorpholine → 4-[N'-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-2-carbonyl)hydrazinocarbonyl]piperidine-1-carboxylic acid tert-butyl ester

HRID 1401818

반응식

HRID 1401818 반응식
[CH3:1][C:2]1([CH3:18])[CH2:11][CH2:10][C:9]([CH3:13])([CH3:12])[C:8]2[CH:7]=[C:6]([C:14]([NH:16][NH2:17])=[O:15])[CH:5]=[CH:4][C:3]1=2.[C:19]([N:26]1[CH2:31][CH2:30]N(C(O)=O)[CH2:28][CH2:27]1)([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20].Cl.CN(C)CCCN=C=NCC.O.ON1C2C=CC=CC=2N=N1.CN1CC[O:62][CH2:61][CH2:60]1>CN(C=O)C.O>[C:22]([O:21][C:19]([N:26]1[CH2:27][CH2:28][CH:60]([C:61]([NH:17][NH:16][C:14]([C:6]2[CH:5]=[CH:4][C:3]3[C:2]([CH3:18])([CH3:1])[CH2:11][CH2:10][C:9]([CH3:12])([CH3:13])[C:8]=3[CH:7]=2)=[O:15])=[O:62])[CH2:30][CH2:31]1)=[O:20])([CH3:23])([CH3:24])[CH3:25]

참가 물질

8

실험 절차

2.2 g (6.22 mmol) of 5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid hydrazide from step b were suspended in 15 ml of DMF together with 1.43 g (6.22 mmol) of 1-Boc-piperazine-4-carboxylic acid (preparation analogous to Bioorganic & Medicinal Chemistry Letters, 2001, vol. 11, #24 p. 3161-3164), 2.41 g (12.45 mmol) of N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride and 867 mg (6.22 mmol) of 1-hydroxybenzotriazole hydrate. 1.40 ml (12.45 mmol) of 4-methylmorpholine were added to the reaction mixture, which was then stirred at room temperature overnight, stirred into 350 ml of water. The resultant precipitate was filtered off with suction, dissolved in DCM, dried, stripped off to dryness and purified by means of flash chromatography on silica gel.

후처리

  1. filtrationThe resultant precipitate was filtered off with suction
  2. dissolutiondissolved in DCM
  3. customdried
  4. custompurified by means of flash chromatography on silica gel

출처 및 근거

ORD 기록
ord-3aa2aad101ef4d2a87f114ba358e0575
출처 데이터셋
uspto-grants-2014_12
특허 번호
US08907098B2

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