1,2-Dichloroethane → HCID 86585259, 화합물

HRID 1018286노트

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HRID 1018286 반응식
C([NH:8][C@H:9]([C:19]([OH:21])=O)[CH2:10][C:11]1[CH:16]=[CH:15][C:14]([OH:17])=[C:13]([I:18])[CH:12]=1)(OC(C)(C)C)=O.[C:22](OC(=O)C)(=[O:24])C.[CH2:29](Cl)[CH2:30]Cl.C1C=CC2N([OH:42])N=NC=2C=1.[NH3:43].C(O)(=O)[CH2:45][C:46]([CH2:51]C(O)=O)([C:48](O)=O)[OH:47]>N1C=CC=CC=1.CN(C1C=CN=CC=1)C.CC(O)C>[C:22]([NH:43][C:19](=[O:21])[C@H:9]([CH2:10][C:11]1[CH:16]=[CH:15][C:14]([O:17][C:29](=[O:42])[CH3:30])=[C:13]([I:18])[CH:12]=1)[NH2:8])([O:47][C:46]([CH3:45])([CH3:48])[CH3:51])=[O:24]

참가 물질

10

실험 절차

To a solution of N-Boc-3-iodotyrosine (0.380 g, 0.93 mmol) in pyridine (1 mL) were added acetic anhydride (105 μL, 1.1 mmol) and DMAP (10 mg, cat). The solution was stirred 1.5 h then diluted in 5% citric acid (20 mL), and the product extracted with EtOAc. The organic solution was evaporated and the residue dissolved in MeCN (4 mL). To the stirred cold (ice bath) solution were added EDC (0.196 g, 1.0 mmol) and HOBt (0.135 g, 1.0 mmol). After stirring for 1 h, a 2 N solution of ammonia in iPrOH (3 mL) was added. The suspension was stirred 1 h at 5° C., the solid was filtered, the filtrate evaporated and the residue purified by flash chromatography (gradient 3-5% MeOH/chloroform) to yield N-Boc-O-acety-3-iodotyrosine amide.

후처리

  1. extractionthe product extracted with EtOAc
  2. customThe organic solution was evaporated
  3. dissolutionthe residue dissolved in MeCN (4 mL)
  4. stirringAfter stirring for 1 h
  5. stirringThe suspension was stirred 1 h at 5° C.
  6. filtrationthe solid was filtered
  7. customthe filtrate evaporated
  8. customthe residue purified by flash chromatography (gradient 3-5% MeOH/chloroform)

출처 및 근거

ORD 기록
ord-50bac30a98c64f61a0a82db87e51a682
출처 데이터셋
uspto-grants-2002_11
특허 번호
US06479508B1

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