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Tetrahydrofuran → HCID 178483007, 화합물

HRID 388140
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HRID 388140 반응식
Br[C:2]1[CH:3]=[CH:4][C:5]2[N:9]=[C:8]([N:10]([CH3:12])[CH3:11])[N:7](C(OC(C)(C)C)=O)[C:6]=2[CH:20]=1.BrC1C=C[C:25]2[N:29]=[C:28](N(C)C)[NH:27][C:26]=2C=1.C(OC(OC(C)(C)C)=O)([O:36][C:37](C)(C)[CH3:38])=O.C(N(CC)CC)C.C[N:57]([C:59]1[CH:64]=[CH:63][CH:62]=[CH:61][N:60]=1)[CH3:58].[O:65]1CCCC1>>[CH3:12][N:10]([CH3:11])[C:8]1[NH:9][C:5]2[CH:4]=[CH:3][C:2]([C:26]3[N:27]=[C:28]4[N:60]([CH2:61][CH:62]5[CH2:63][CH2:64][O:36][CH2:37][CH2:38]5)[C:59](=[O:65])[NH:57][C:58]4=[N:29][CH:25]=3)=[CH:20][C:6]=2[N:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 6

HCID 8028TetrahydrofuranHCID 8471TriethylamineHCID 218852-DimethylaminopyridineHCID 90495Di-tert-butyl dicarbonateHCID 594745206-Bromo-N,N-dimethyl-1H-benzimidazol-2-amineHCID 66699934HCID 66699934, 화합물

생성물 1

HCID 178483007
HCID 178483007, 화합물
수율 54%

실험 절차

tert-Butyl 6-bromo-2-(dimethylamino)-1H-benzo[d]imidazole-1-carboxylate. A solution of 6-bromo-N,N-dimethyl-1H-benzo[d]imidazol-2-amine (0.5 g, 2.08 mmol), di-tert-butyl dicarbonate (0.54 g, 2.5 mmol), triethylamine (0.35 mL, 2.55 mmol) and dimethylaminopyridine (few crystals) in anhydrous tetrahydrofuran (10 mL) was allowed to stir at room temperature overnight. The reaction mixture was concentrated under reduced pressure and the crude product was purified by Biotage chromatography (0-55% ethyl acetate in hexanes) to provide the desired product (0.32 g, 54%) as a white solid. MS (ESI) m/z 341.3 [M+1]+.

후처리

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. customthe crude product was purified by Biotage chromatography (0-55% ethyl acetate in hexanes)

출처 및 근거

ORD 기록
ord-419f85ebb60e4f729c7304ed577cde50
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08372976B2

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