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Hydrochloric Acid → HCID 20288856, 화합물

HRID 1395420
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HRID 1395420 반응식
[ClH:1].[NH2:2][C:3]1[N:8]=[C:7]([NH2:9])[C:6]([CH2:10][C:11]2[CH:16]=[C:15]([O:17][CH3:18])[C:14]([C:19]([CH3:21])=[CH2:20])=[C:13]([O:22][CH3:23])[CH:12]=2)=[CH:5][N:4]=1>CO>[ClH:1].[NH2:2][C:3]1[N:8]=[C:7]([NH2:9])[C:6]([CH2:10][C:11]2[CH:12]=[C:13]([O:22][CH3:23])[C:14]([C:19]([CH3:21])=[CH2:20])=[C:15]([O:17][CH3:18])[CH:16]=2)=[CH:5][N:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 479082HCID 479082, 화합물

생성물 1

HCID 20288856HCID 20288856, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

3.3 Ml. of 1-N hydrochloric acid were added to a solution of 0.9 g. of 2,4-diamino-5-(4-isopropenyl-3,5-dimethoxybenzyl)-pyrimidine in 100 ml. of methanol. The solution was concentrated to 25 ml. and, after cooling, the crystals were removed by filtration under suction and dried. The resulting 2,4-diamino-5-(4-isopropenyl-3,5-dimethoxybenzyl)-pyrimidine hydrochloride melts at above 300° C.

후처리

  1. concentrationThe solution was concentrated to 25 ml
  • temperatureand, after cooling
  • customthe crystals were removed by filtration under suction
  • customdried
  • 출처 및 근거

    ORD 기록
    ord-54aaa4966c664126bc7a27e9b5309c25
    출처 데이터셋
    uspto-grants-1980_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04203980

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