1-Hydroxybenzotriazole → N-((1R)-1-(N-((1R)-2-(2-Fluorophenyl)-1-(methylcarbamoyl)ethyl)-N-methyl-carbamoyl)-2-(2-naphthyl)ethyl)-N-methylcarbamic acid tert-butylester

HRID 495789

반응식

HRID 495789 반응식
[C:1]([O:5][C:6]([NH:8][CH2:9][C:10]([OH:12])=O)=[O:7])([CH3:4])([CH3:3])[CH3:2].ON1C2C=CC=C[C:17]=2N=N1.Cl.CN(C)CCCN=C=NCC.[F:35][C:36]1[CH:41]=[CH:40][CH:39]=[CH:38][C:37]=1[CH2:42][C@@H:43]([NH:48][CH3:49])[C:44]([NH:46][CH3:47])=[O:45].C(N(C(C)C)CC)(C)C.C(OC(CNC([CH2:72][C:73]1[CH:82]=[CH:81][C:80]2[C:75](=[CH:76][CH:77]=[CH:78][CH:79]=2)[CH:74]=1)C(O)=O)=O)(C)(C)C.ON1C2N=CC=CC=2N=N1>C(Cl)Cl>[C:1]([O:5][C:6](=[O:7])[N:8]([C@@H:9]([C:10](=[O:12])[N:48]([C@@H:43]([C:44](=[O:45])[NH:46][CH3:47])[CH2:42][C:37]1[CH:38]=[CH:39][CH:40]=[CH:41][C:36]=1[F:35])[CH3:49])[CH2:72][C:73]1[CH:82]=[CH:81][C:80]2[C:75](=[CH:76][CH:77]=[CH:78][CH:79]=2)[CH:74]=1)[CH3:17])([CH3:2])([CH3:3])[CH3:4]

참가 물질

9

반응물 7

HCID 757711-HydroxybenzotriazoleHCID 78288N-(tert-butoxycarbonyl)glycineHCID 81531DiisopropylethylamineHCID 181649HOAtHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride2회HCID 223270012-(Tert-butoxycarbonylmethylamino)-3-(2-naphthyl)propionic acidHCID 54111884(2R)-3-(2-Fluorophenyl)-N-methyl-2-(methylamino)propionamide

생성물 1

HCID 53671638N-((1R)-1-(N-((1R)-2-(2-Fluorophenyl)-1-(methylcarbamoyl)ethyl)-N-methyl-carbamoyl)-2-(2-naphthyl)ethyl)-N-methylcarbamic acid tert-butylester수율 69%

시약·촉매·용매 1

HCID 6344Dichloromethane용매3회

실험 절차

Tert-Butoxycarbonylaminoacetic acid (0.18 g; 2.39 mmol) was dissolved in methylene chloride (20 mL). 1-Hydroxybenzotriazole (0.32 g; 2.39 mmol) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.55 g; 2.87 mmol) were added and the reaction mixture was stirred for 15 min at room temperature. (2R)-3-(2-Fluorophenyl)-N-methyl-2-(methylamino)propionamide (1.0 g; 4.78 mmol) and diisopropylethylamine (0.9 mL; 5.26 mmol) was added and the reaction mixture was stirred for 12 hours at room temperature. A mixture of 2-(tert-butoxycarbonylmethylamino)-3-(2-naphthyl)propionic acid (0.78 g; 2.39 mmol), 1-hydroxy-7-azabenzotriazole (0.33 g; 2.39 mmol) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.55 g; 2.87 mmol) were dissolved in methylene chloride (20 mL) and added to the reaction mixture. The reaction mixture was stirred for 12 hours at room temperature. Methylene chloride (50 mL) was added and the reaction mixture was washed with water (30 mL), an aqueous solution of sodium hydrogen sulfate (10%; 30 mL), an aqueous solution of sodium hydrogen carbonate/sodium carbonate (pH 9; 30 mL) and water (30 mL) and dried (magnesium sulfate). The solvent was removed in vacuo and the residue was chromatographed on silica (2.5×30 cm) using ethyl acetate/heptane (2:1) as eluent to afford 0.86 g of N-((1R)-1-(N-((1R)-2-(2-fluorophenyl)-1-(methylcarbamoyl)ethyl)-N-methylcarbamoyl)-2-(2-naphthyl)ethyl)-N-methyl-carbamic acid tert-butylester.

후처리

  1. stirringthe reaction mixture was stirred for 12 hours at room temperature
  2. additionadded to the reaction mixture
  3. stirringThe reaction mixture was stirred for 12 hours at room temperature
  4. washthe reaction mixture was washed with water (30 mL)
  5. dry with materialan aqueous solution of sodium hydrogen sulfate (10%; 30 mL), an aqueous solution of sodium hydrogen carbonate/sodium carbonate (pH 9; 30 mL) and water (30 mL) and dried (magnesium sulfate)
  6. customThe solvent was removed in vacuo
  7. customthe residue was chromatographed on silica (2.5×30 cm)

출처 및 근거

ORD 기록
ord-d64104bcf41b4169b1ca0270290a763d
출처 데이터셋
uspto-grants-2005_09
특허 번호
US06939880B2

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