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Ammonia → 5-iodo-2-pyrrolidin-1-yl-1H-benzimidazole

HRID 2112825
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HRID 2112825 반응식
Br[C:2]1[CH:15]=[CH:14][C:5]2[NH:6][C:7]([N:9]3[CH2:13][CH2:12][CH2:11][CH2:10]3)=[N:8][C:4]=2[CH:3]=1.[Na+].[I-:17].NCCN.N>O.[Cu]I.O1CCOCC1>[I:17][C:2]1[CH:15]=[CH:14][C:5]2[NH:6][C:7]([N:9]3[CH2:13][CH2:12][CH2:11][CH2:10]3)=[N:8][C:4]=2[CH:3]=1
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참가 물질

8

반응물 4

HCID 222AmmoniaHCID 3301EthylenediamineHCID 5238Sodium IodideHCID 178419330HCID 178419330, 화합물

생성물 1

HCID 1785065395-iodo-2-pyrrolidin-1-yl-1H-benzimidazole

시약·촉매·용매 3

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)촉매
HCID 962Water용매
HCID 312751,4-Dioxane용매

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온도
110 °C

실험 절차

0.48 g (1.8 mmol) of 5-bromo-2-pyrrolidin-1-yl-1H-benzimidazole and 34 mg (0.18 mmol) of CuI are placed in a round flask. The reaction vessel is flushed with argon. Then 0.54 g (3.6 mmol) of NaI, 32 mg (0.36 mmol) of dimethylenediamine, and 3 mL of 1,4-dioxane are added under argon. The reaction mixture is stirred for 14 hours at 110° C. Subsequently, the cooled reaction mixture is combined with concentrated ammonia solution, diluted with water, and the precipitate formed is filtered off. The solid is stirred with methanol and again filtered. Yield: 0.3 g (53% of theoretical); C11H12IN3 (M=313.13); calc.: molpeak (M+H)+: 314; found: molpeak (M)+: 314.

후처리

  1. customThe reaction vessel is flushed with argon
  2. customSubsequently, the cooled reaction mixture
  3. customthe precipitate formed
  4. filtrationis filtered off
  5. stirringThe solid is stirred with methanol
  6. filtrationagain filtered

출처 및 근거

ORD 기록
ord-03671c1e21084e4ab6761c9ecacc257f
출처 데이터셋
uspto-grants-2009_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07524862B2

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