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1-Hydroxybenzotriazole → (6S)-6-(5-chloro-2-methoxybenzyl)-1-(2,4,6-trimethoxybenzyl)-1,4-diazepan-2,5-dione

HRID 554828
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HRID 554828 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:32][CH3:33])=[C:6]([CH:31]=1)[CH2:7][C@@H:8]([CH2:16][NH:17][CH2:18][C:19]1[C:24]([O:25][CH3:26])=[CH:23][C:22]([O:27][CH3:28])=[CH:21][C:20]=1[O:29][CH3:30])[C:9]([NH:11][CH2:12][C:13]([OH:15])=O)=[O:10].ON1C2C=CC=CC=2N=N1.Cl.CN(C)CCCN=C=NCC>C(#N)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:32][CH3:33])=[C:6]([CH:31]=1)[CH2:7][C@H:8]1[CH2:16][N:17]([CH2:18][C:19]2[C:24]([O:25][CH3:26])=[CH:23][C:22]([O:27][CH3:28])=[CH:21][C:20]=2[O:29][CH3:30])[C:13](=[O:15])[CH2:12][NH:11][C:9]1=[O:10]
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참가 물질

5

반응물 3

HCID 757711-HydroxybenzotriazoleHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 67460156HCID 67460156, 화합물

생성물 1

HCID 66935303(6S)-6-(5-chloro-2-methoxybenzyl)-1-(2,4,6-trimethoxybenzyl)-1,4-diazepan-2,5-dione

시약·촉매·용매 1

HCID 6342Acetonitrile용매

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온도
40 °C

실험 절차

To a solution of N-{(2S)-2-(5-chloro-2-methoxybenzyl)-3-[(2,4,6-trimethoxybenzyl)amino]propanoyl}glycine (1g) in acetonitrile (30 ml), 1-hydroxy benzotriazole (421 mg) was added at room temperature. The mixture was stirred at 40° C. for 20 minutes, then N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (598 mg) was added to the reaction solution, and the mixture was stirred for 2 hours. After the reaction solution was concentrated in vacuo, toluene was added to the obtained residue, and the resulting mixture was washed with 6% aqueous sodium bicarbonate and saturated brine. The organic layer was concentrated in vacuo, then the obtained residue was purified by silica gel column chromatography to obtain the title compound (894 mg) as a colorless crystal.

후처리

  1. stirringthe mixture was stirred for 2 hours
  2. concentrationAfter the reaction solution was concentrated in vacuo, toluene
  3. additionwas added to the obtained residue
  4. washthe resulting mixture was washed with 6% aqueous sodium bicarbonate and saturated brine
  5. concentrationThe organic layer was concentrated in vacuo
  6. customthe obtained residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-c73109fc85b946e7971aeebbc131558b
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08049006B2

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