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Hydrochloric Acid → 5-Chloro-4-{2-[4-(2-ethoxyethyl)-2-methylphenoxy]ethylamino}-6-methylpyrimidine hydrochloride

HRID 231116
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인쇄 미리보기

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HRID 231116 반응식
[Cl:1][C:2]1[C:3]([NH:9][CH2:10][CH2:11][O:12][C:13]2[CH:18]=[CH:17][C:16]([CH2:19][CH2:20][O:21][CH2:22][CH3:23])=[CH:15][C:14]=2[CH3:24])=[N:4][CH:5]=[N:6][C:7]=1[CH3:8].Cl>O>[ClH:1].[Cl:1][C:2]1[C:3]([NH:9][CH2:10][CH2:11][O:12][C:13]2[CH:18]=[CH:17][C:16]([CH2:19][CH2:20][O:21][CH2:22][CH3:23])=[CH:15][C:14]=2[CH3:24])=[N:4][CH:5]=[N:6][C:7]=1[CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 139099695-Chloro-4-{2-[4-(2-ethoxyethyl)-2-methylphenoxy]ethylamino}-6-methylpyrimidine

생성물 1

HCID 200345095-Chloro-4-{2-[4-(2-ethoxyethyl)-2-methylphenoxy]ethylamino}-6-methylpyrimidine hydrochloride수율 188.4%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

5.0 g of 5-chloro-4-{2-[4-(2-ethoxyethyl)-2-methylphenoxy]ethylamino}-6-methylpyrimidine (powder) were suspended in 10 ml of water, and 5 ml of concentrated aqueous hydrochloric acid were added dropwise thereto. After this addition, the mixture was stirred for 30 minutes, and cooled to separate the crystals. These crystals were collected by filtration and washed with cold water and toluene, in that order, to give 5.2 g of the title compound as colorless needles melting at 123°-124° C.

후처리

  1. additionAfter this addition
  2. temperaturecooled
  3. customto separate the crystals
  4. filtrationThese crystals were collected by filtration
  5. washwashed with cold water and toluene, in that order

출처 및 근거

ORD 기록
ord-20437f4510864f1aae23711a4612b5f0
출처 데이터셋
uspto-grants-1989_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04845097

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