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Hydrochloric Acid → 4-Chloro-1H-benzo[d]imidazol-5-amine

HRID 1157402
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HRID 1157402 반응식
[Cl:1][C:2]1[C:10]2[N:9]=[CH:8][NH:7][C:6]=2[CH:5]=[CH:4][C:3]=1[NH:11]C(=O)C.C(O)C.Cl>O>[Cl:1][C:2]1[C:10]2[N:9]=[CH:8][NH:7][C:6]=2[CH:5]=[CH:4][C:3]=1[NH2:11]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 702EthanolHCID 4083933HCID 4083933, 화합물

생성물 1

HCID 129684544-Chloro-1H-benzo[d]imidazol-5-amine

시약·촉매·용매 1

HCID 962Water용매

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온도
85 °C

실험 절차

58 mg (0.277 mmol) of N-(4-chloro-1H-benzimidazol-5-yl)acetamide (24-1) was suspended in a mixture of water, ethanol and concentrated HCl (0.06:1:0.4) for a total of 1 mL. The suspension was stirred and heated at 85° C. under nitrogen for 1 hour and after this time everything was soluble. The heat was turned off the solution was stirred overnight. The reaction was quenched with saturated NaHCO3. The pH was adjusted to 8 by adding solid NaHCO3 and Na2CO3. Extracted the reaction with ethyl acetate, dried, filtered and evaporated to recover the desired product 24-2. MS (M+1): measured 168.2; theoretical 167.0. 1H NMR (CD3OD): 6.75 (dd, 1H), 7.37 (d, 1H), 7.93 (s, 1H).

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. stirringwas stirred overnight
  2. customThe reaction was quenched with saturated NaHCO3
  3. additionby adding solid NaHCO3 and Na2CO3
  4. extractionExtracted
  5. customthe reaction with ethyl acetate
  6. customdried
  7. filtrationfiltered
  8. customevaporated
  9. customto recover the desired product 24-2

출처 및 근거

ORD 기록
ord-50cae2dc47b24e4a85610be4e129b2d7
출처 데이터셋
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07807684B2

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