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Dimethylformamide → methyl N-{[4-({[(benzyloxy)carbonyl]amino}methyl)cyclohexyl]carbonyl}-L-norleucinate

HRID 488655
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HRID 488655 반응식
[CH2:1]([O:8][C:9]([NH:11][CH2:12][CH:13]1[CH2:18][CH2:17][CH:16]([C:19]([OH:21])=O)[CH2:15][CH2:14]1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CN(C(ON1N=[N:37][C:32]2[CH:33]=[CH:34][CH:35]=[CH:36][C:31]1=2)=[N+](C)C)C.[B-](F)(F)(F)F.C1C=CC2N([OH:53])N=NC=2C=1.C(N(CC)CC)C.CN([CH:64]=[O:65])C>O>[CH2:1]([O:8][C:9]([NH:11][CH2:12][CH:13]1[CH2:14][CH2:15][CH:16]([C:19]([NH:37][C@H:32]([C:31]([O:65][CH3:64])=[O:53])[CH2:33][CH2:34][CH2:35][CH3:36])=[O:21])[CH2:17][CH2:18]1)=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
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참가 물질

7

반응물 5

HCID 6228DimethylformamideHCID 8471TriethylamineHCID 757711-HydroxybenzotriazoleHCID 2733207O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 3723035Cbz-trans-4-(aminomethyl)cyclohexanecarboxylic acid

생성물 1

HCID 69803360
methyl N-{[4-({[(benzyloxy)carbonyl]amino}methyl)cyclohexyl]carbonyl}-L-norleucinate
수율 77%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To a stirring mixture of 4-({[(benzyloxy)carbonyl]amino}methyl)cyclohexanecarboxylic acid (750 mg, 2.57 mmol), TBTU (1.08 g, 3.34 mmol), and HOBT (55 mg, 0.03 mmol) in DMF (15 mL) was added the norleucine OMe HCl (411 mg, 2.83 mmol), followed by addition of triethylamine (898 μL, 6.43 mmol). The resulting mixture was then stirred at ambient temperature for 2 hours, diluted with water and the resulting precipitate was collected by filtration and dried in a vacuum oven to provide the titled compound (830 mg, 1.98 mmol, 77%).

후처리

  1. filtrationthe resulting precipitate was collected by filtration
  2. customdried in a vacuum oven

출처 및 근거

ORD 기록
ord-d3e4ea6171f64419853ca8606e5dd651
출처 데이터셋
uspto-grants-2005_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06972340B2

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