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Cyanuric chloride → 4,6-dichloro-N-[(2R)-2-phenylpropyl]-1,3,5-triazin-2-amine

HRID 1671759
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HRID 1671759 반응식
[N:1]1[C:8]([Cl:9])=[N:7][C:5](Cl)=[N:4][C:2]=1[Cl:3].[CH3:10][C@H:11]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[CH2:12][NH2:13].[OH-].[Na+]>CC#N.O>[Cl:9][C:8]1[N:1]=[C:2]([Cl:3])[N:4]=[C:5]([NH:13][CH2:12][C@@H:11]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH3:10])[N:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7954Cyanuric chlorideHCID 14798Sodium HydroxideHCID 1547949(R)-(+)-beta-Methylphenethylamine

생성물 1

HCID 866443924,6-dichloro-N-[(2R)-2-phenylpropyl]-1,3,5-triazin-2-amine

시약·촉매·용매 1

HCID 18373917Acetonitrile--water (1/1)용매

실험 절차

A mixture of cyanuric chloride (75 mg, 0.407 mmol, 1 equivalent) in CH3CN/H2O (1/1, 5 ml) was cooled to 0° C. (R)-(+)-beta-methylphenethylamine (55 mg, 0.407 mmol, 1 equivalent) was added, followed by 1N NaOH (0.366 ml). LCMS analysis showed the complete consumption of the 2,4,6-trichloro-1,3,5-triazine. The crude product was used in the next step. MS (ES+): m/e 283.06 [M+H]+.

후처리

  1. additionwas added
  2. customthe complete consumption of the 2,4,6-trichloro-1,3,5-triazine

출처 및 근거

ORD 기록
ord-3d80e7034fff4ee7a1387ffc13725a5d
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07994317B2

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