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Hydrochloric Acid → 4-(1H-Imidazol-2-yl)piperidine dihydrochloride

HRID 1725770
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반응식

HRID 1725770 반응식
[NH:1]1[CH:5]=[CH:4][N:3]=[C:2]1[CH:6]1[CH2:11][CH2:10][N:9](C(OC(C)(C)C)=O)[CH2:8][CH2:7]1.[ClH:19]>CO>[ClH:19].[ClH:19].[NH:1]1[CH:5]=[CH:4][N:3]=[C:2]1[CH:6]1[CH2:11][CH2:10][NH:9][CH2:8][CH2:7]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 17840015tert-butyl 4-(1H-imidazol-2-yl)piperidine-1-carboxylate

생성물 1

HCID 132811914-(1H-Imidazol-2-yl)piperidine dihydrochloride

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of tert-butyl 4-(1H-imidazol-2-yl)piperidine-1-carboxylate (5.5 g) in methanol was saturated with HCl and the mixture was left standing overnight. Evaporation give the product in quantitative yield. 1H NMR (400 MHz, D2O): 7.29 (s, 2H), 3.51 (br. d, J=13 Hz, 2H), 3.47-3.40 (m, 1H), 3.12 (br. t, J=13 Hz, 2H), 2.29 (br. d, J=14 Hz, 2H), 2.04-1.92 (m, 21).

후처리

  1. waitthe mixture was left
  2. customEvaporation
  3. customgive the product in quantitative yield

출처 및 근거

ORD 기록
ord-73dc8929c73247ff81ff4ce59d50f92a
출처 데이터셋
uspto-grants-2009_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07491737B2

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