Triethylamine → Benzyl 2-[({[2-(diisopropylamino)ethyl]amino}carbonyl)amino]ethylcarbamate

HRID 10461노트

반응식

HRID 10461 반응식
Cl.[NH2:2][CH2:3][CH2:4][NH:5][C:6](=[O:15])[O:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[CH:16]([N:19]([CH:30]([CH3:32])[CH3:31])[CH2:20][CH2:21][NH:22][C:23](N1C=CN=C1)=[O:24])([CH3:18])[CH3:17].C(N(CC)CC)C>ClCCl>[CH:30]([N:19]([CH:16]([CH3:18])[CH3:17])[CH2:20][CH2:21][NH:22][C:23]([NH:2][CH2:3][CH2:4][NH:5][C:6](=[O:15])[O:7][CH2:8][C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=1)=[O:24])([CH3:32])[CH3:31]

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 12715871Benzyl N-(2-aminoethyl)carbamate hydrochlorideHCID 21978296N-[2-(diisopropylamino)ethyl]-1H-imidazole-1-carboxamide

생성물 1

HCID 21978301Benzyl 2-[({[2-(diisopropylamino)ethyl]amino}carbonyl)amino]ethylcarbamate수율 109.6%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of benzyl 2-aminoethylcarbamate hydrochloride (4.33 g, 18.8 mmol), N-[2-(diisopropylamino)ethyl]-1H-imidazole-1-carboxamide (Preparation 19) (3.73 g, 15.64 mmol) and triethylamine (2.62 ml, 18.8 mmol) in dichloromethane (100 ml) was heated under reflux for 14 hours. The solution was allowed to cool to room temperature and then washed with water (20 ml). The aqueous layer was separated and extracted with more dichloromethane (20 ml). The combined organic layers were dried over anhydrous magnesium sulfate and solvent evaporated under reduced pressure to give the title compound as a yellow oil (6.25 g).

후처리

  1. temperatureunder reflux for 14 hours
  2. washwashed with water (20 ml)
  3. customThe aqueous layer was separated
  4. extractionextracted with more dichloromethane (20 ml)
  5. dry with materialThe combined organic layers were dried over anhydrous magnesium sulfate and solvent
  6. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-1eb4ad4101bd408cab4df1eea911d020
출처 데이터셋
uspto-grants-2006_08
특허 번호
US07094769B2

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