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Potassium Carbonate → 6-Chloro-9-(3,4,5-trimethyl-pyridin-2-ylmethyl)-9H-purin-2-ylamine

HRID 722111
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인쇄 미리보기

반응식

HRID 722111 반응식
Br[CH2:2][C:3]1[C:8]([CH3:9])=[C:7]([CH3:10])[C:6]([CH3:11])=[CH:5][N:4]=1.[Cl:12][C:13]1[N:21]=[C:20]([NH2:22])[N:19]=[C:18]2[C:14]=1[N:15]=[CH:16][NH:17]2.C([O-])([O-])=O.[K+].[K+]>>[Cl:12][C:13]1[N:21]=[C:20]([NH2:22])[N:19]=[C:18]2[C:14]=1[N:15]=[CH:16][N:17]2[CH2:2][C:3]1[C:8]([CH3:9])=[C:7]([CH3:10])[C:6]([CH3:11])=[CH:5][N:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 11430Potassium CarbonateHCID 167350512-Bromomethyl-3,4,5-trimethyl-pyridineHCID 1785084356-chloro-1H-purin-2-amine

생성물 1

HCID 167367676-Chloro-9-(3,4,5-trimethyl-pyridin-2-ylmethyl)-9H-purin-2-ylamine

실험 절차

The compound was obtained by reacting 2-bromomethyl-3,4,5-trimethyl-pyridine with 6-chloro-9H-purin-2-ylamine in the presence of K2CO3 at 5° C. for 0.5 h as described in the general procedure 1.1. HPLC Rt: 3.903 min. 1H-NMR (CDCl3): δ 8.18 (s, 1H), 7.84 (s, 1H), 5.38 (s, 2H), 5.08 (s, 2H), 2.29 (s, 3H), 2.27 (s, 3H), 2.22 (s, 3H).

후처리

  1. customThe compound was obtained
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • customat 5° C.
  • customfor 0.5 h
  • 출처 및 근거

    ORD 기록
    ord-e345e7145483418ba5d3dfa96b8eab7f
    출처 데이터셋
    uspto-grants-2006_11
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07138401B2

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