Potassium Carbonate → Tert-butyl 2-((6-bromohexyl)(2-tert-butoxybenzyl)amino)ethylcarbamate

HRID 403121노트

반응식

HRID 403121 반응식
[C:1]([O:5][C:6]1[CH:23]=[CH:22][CH:21]=[CH:20][C:7]=1[CH2:8][NH:9][CH2:10][CH2:11][NH:12][C:13](=[O:19])[O:14][C:15]([CH3:18])([CH3:17])[CH3:16])([CH3:4])([CH3:3])[CH3:2].[Br:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30]Br.C([O-])([O-])=O.[K+].[K+]>CC#N>[Br:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][N:9]([CH2:8][C:7]1[CH:20]=[CH:21][CH:22]=[CH:23][C:6]=1[O:5][C:1]([CH3:2])([CH3:3])[CH3:4])[CH2:10][CH2:11][NH:12][C:13](=[O:19])[O:14][C:15]([CH3:16])([CH3:17])[CH3:18]

참가 물질

5

실험 절차

Compound 14 (3.56 g, 14.6 mmol), 1,6-dibromohexane (35.3 g, 146 mmol) and K2CO3 (2 g, 14.6 mmol) were added to 50 mL CH3CN, and the solution was stirred for 48 h. The solvent was evaporated to dryness and the residue was dissolved in a minimum amount of CH2Cl2 followed by purification via silica gel chromatographed, eluting with a 2% methanolic NH3 (7 M NH3 in methanol/98% CH2Cl2 yield the desired product as a pale yellow oil (64%). 1H NMR (CDCl3) δ 7.354 (dd, 1H, Ar), 7.121 (ddd, 1H, Ar), 7.013 (d, 1H, Ar), 6.986 (t, 1H, Ar), 3.569 (s, 2H, —CH2), 3.351 (t, 2H, —CH2—), 3.145 (d, 2H, —CH2—), 2.507 (t, 2H, —CH2—), 2.399 (t, 2H, —CH2—), 1.805 (p, 2H, —CH2—),1.447 (p, 2H, —CH2—), 1.409 (s, 9H, —C(CH3)3), 1.372 (s, 9H, —C(CH3)3), 1.362 (p, 2H, —CH2—), 1.254 (p, 2H, —CH2—). Mass Spec.=485.48 (M+H)+.

후처리

  1. customThe solvent was evaporated to dryness
  2. dissolutionthe residue was dissolved in a minimum amount of CH2Cl2
  3. customfollowed by purification via silica gel
  4. customchromatographed
  5. washeluting with a 2% methanolic NH3 (7 M NH3 in methanol/98% CH2Cl2

출처 및 근거

ORD 기록
ord-2527b7e2baf54d2596d1a6d9574a2b44
출처 데이터셋
uspto-grants-2014_06
특허 번호
US08747810B2

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