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Hydrochloric Acid → HCID 68644042, 화합물

HRID 2388689
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HRID 2388689 반응식
[N:1]1([CH2:5][C:6]2[S:14][C:13]3[CH2:12][CH2:11][N:10](C(OC(C)(C)C)=O)[CH2:9][C:8]=3[CH:7]=2)[CH2:4][CH2:3][CH2:2]1.[ClH:22]>CO>[ClH:22].[ClH:22].[N:1]1([CH2:5][C:6]2[S:14][C:13]3[CH2:12][CH2:11][NH:10][CH2:9][C:8]=3[CH:7]=2)[CH2:4][CH2:3][CH2:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

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HCID 313Hydrochloric AcidHCID 86635669Tert-Butyl 2-(azetidin-1-ylmethyl)-6,7-dihydrothieno[3,2-c]pyridine-5(4H)-carboxylate

생성물 1

HCID 68644042HCID 68644042, 화합물

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

tert-Butyl 2-(azetidin-1-ylmethyl)-6,7-dihydrothieno[3,2-c]pyridine-5(4H)-carboxylate (0.28 g, 0.908 mmol) was dissolved in methanol (1 ml) and HCl in methanol (1.25 M, 3.63 ml, 4.54 mmol) was added. The reaction mixture was heated at reflux for 1 h. After cooling to room temperature the solvent was removed in vacuo. The crude product was re-dissolved in ethanol, diethylether was added and the mixture was stirred at 0° C. for 20 min. The solid was collected by filtration, washed with diethylether and dried in vacuo. Yield: 0.2 g (78%).

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후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux for 1 h
  3. customwas removed in vacuo
  4. dissolutionThe crude product was re-dissolved in ethanol
  5. additiondiethylether was added
  6. filtrationThe solid was collected by filtration
  7. washwashed with diethylether
  8. customdried in vacuo

출처 및 근거

ORD 기록
ord-a4faa13a2d9d478aaa43e4012b2e1960
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08268814B2

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