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Diethyl Ether → HCID 70059617, 화합물

HRID 2230292
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HRID 2230292 반응식
[C:1]([NH:8][C@H:9]([C:27](O)=[O:28])[CH2:10][C:11]1[CH:16]=[CH:15][C:14]([O:17][CH2:18][C:19]2[C:24]([Cl:25])=[CH:23][CH:22]=[CH:21][C:20]=2[Cl:26])=[CH:13][CH:12]=1)([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[C:54]([NH2:58])([CH3:57])([CH3:56])[CH3:55].CCOCC>CN(C=O)C.CCN(C(C)C)C(C)C>[C:4]([O:3][C:1](=[O:2])[NH:8][C@H:9]([C:27](=[O:28])[NH:58][C:54]([CH3:57])([CH3:56])[CH3:55])[CH2:10][C:11]1[CH:16]=[CH:15][C:14]([O:17][CH2:18][C:19]2[C:24]([Cl:25])=[CH:23][CH:22]=[CH:21][C:20]=2[Cl:26])=[CH:13][CH:12]=1)([CH3:6])([CH3:5])[CH3:7]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 3283Diethyl EtherHCID 6385Tert-ButylamineHCID 2733084Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 11133964L-Tyrosine, O-[(2,6-dichlorophenyl)methyl]-N-[(1,1-dimethylethoxy)carbonyl]-

생성물 1

HCID 70059617HCID 70059617, 화합물수율 69.4%

시약·촉매·용매

2
HCID 6228Dimethylformamide용매HCID 81531Diisopropylethylamine용매

반응 조건

온도
0 °C

실험 절차

A solution of BOC-O-(2,6-dichlorobenzyl)-L-tyrosine (Bachem, 2.00 g, 4.54 mmol) in 20 mL of DMF and iPr2NEt (1.6 mL) was cooled to 0° C. and treated with HBTU (1.72 g, 4.54 mmol). The resulting solution was stirred at 0° C. for 30 minutes and treated with tert-butyl amine (0.48 mL, 4.54 mmol). The resulting solution was stirred overnight. The reaction mixture was poured into ether (100 mL) and washed sequentially with saturated aqueous NaHCO3 solution (20 mL) and brine (4×20 mL). The organic phase was collected and dried (MgSO4) and concentrated. The crude reaction product was purified by chromatography (silica gel, 2:1 heptane/EtOAc). The solid obtained was crystallized from hot heptane, collected by suction filtration and dried to give the title compound as a white solid (1.56 g, 69%), mp=82-86° C.

후처리

  1. stirringThe resulting solution was stirred overnight
  2. washwashed sequentially with saturated aqueous NaHCO3 solution (20 mL) and brine (4×20 mL)
  3. customThe organic phase was collected
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated
  6. customThe crude reaction product
  7. customwas purified by chromatography (silica gel, 2:1 heptane/EtOAc)
  8. customThe solid obtained
  9. customwas crystallized from hot heptane
  10. filtrationcollected by suction filtration
  11. customdried

출처 및 근거

ORD 기록
ord-e0ea3705da364abbadc5e11464b48aa0
출처 데이터셋
uspto-grants-2002_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06423689B1

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