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Oms-210 → 5-Chloro-2-(1-homopiperazinyl)-7-methylbenzoxazole hydrochloride

HRID 1824712
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HRID 1824712 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH3:18])[C:5]2[O:9][C:8]([N:10]3[CH2:16][CH2:15][CH2:14][NH:13][CH2:12][CH2:11]3)=[N:7][C:6]=2[CH:17]=1.Cl.C(OCC)(=O)C>C(OCC)(=O)C>[ClH:1].[Cl:1][C:2]1[CH:3]=[C:4]([CH3:18])[C:5]2[O:9][C:8]([N:10]3[CH2:16][CH2:15][CH2:14][NH:13][CH2:12][CH2:11]3)=[N:7][C:6]=2[CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 9903419Oms-210HCID 21866389Hydrogen chloride-ethyl acetate

생성물 1

HCID 221423235-Chloro-2-(1-homopiperazinyl)-7-methylbenzoxazole hydrochloride수율 212.5%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

5-Chloro-2-(1-homopiperazinyl)-7-methylbenzoxazole (12 g) was dissolved in ethyl acetate (200 mL), and the solution was added dropwise with 4 N hydrochloric acid/ethyl acetate (16.9 mL, Kokusan Kagaku Co., Ltd.) at room temperature with stirring. After the addition, the mixture was stirred for 30 minutes with ice cooling, and the produced colorless precipitates were collected by filtration. The precipitates were dried at 35 C.° under reduced pressure for 4 hours to obtain the title compound (14.5 g).

후처리

  1. additionAfter the addition
  2. stirringthe mixture was stirred for 30 minutes with ice cooling
  3. customthe produced colorless precipitates
  4. filtrationwere collected by filtration
  5. customThe precipitates were dried at 35 C.° under reduced pressure for 4 hours

출처 및 근거

ORD 기록
ord-d2adcb502f9e43f38f50f34d635ae291
출처 데이터셋
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07045516B1

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