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Sodium Azide → 4-(Azidomethyl)-2,6-dihydroxymethyl-s-triazine

HRID 495887
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HRID 495887 반응식
C1(C)C=CC(S([CH2:10][C:11]2[N:16]=[C:15]([CH2:17][OH:18])[N:14]=[C:13]([CH2:19][OH:20])[N:12]=2)(=O)=O)=CC=1.[N-:22]=[N+:23]=[N-:24].[Na+]>CN(C=O)C>[N:22]([CH2:10][C:11]1[N:12]=[C:13]([CH2:19][OH:20])[N:14]=[C:15]([CH2:17][OH:18])[N:16]=1)=[N+:23]=[N-:24]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 33557Sodium AzideHCID 223236944-(p-Toluenesulfonylmethyl)-2,6-dihydroxymethyl-s-triazine

생성물 1

HCID 223236434-(Azidomethyl)-2,6-dihydroxymethyl-s-triazine

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
50 °C

실험 절차

4-(p-Toluenesulfonylmethyl)-2,6-dihydroxymethyl-s-triazine is dissolved in DMF and sodium azide (1.1 eq.) is added. The reaction mixture is heated to 50° C. for 4 hours. The DMF is removed under reduced pressure and the residue is partitioned between CH2Cl2 and water. The CH2Cl2 layer is separated and the water layer is extracted several times with CH2Cl2. The CH2Cl2 layers are combined, dried (MgSO4), and concentrated. The resultant residue is purified by silica gel flash column chromatography to give 4-(azidomethyl)-2,6-dihydroxymethyl-s-triazine.

후처리

  1. customThe DMF is removed under reduced pressure
  2. customthe residue is partitioned between CH2Cl2 and water
  3. customThe CH2Cl2 layer is separated
  4. extractionthe water layer is extracted several times with CH2Cl2
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated
  7. customThe resultant residue is purified by silica gel flash column chromatography

출처 및 근거

ORD 기록
ord-29d4037771374b3b8268aa2005f967be
출처 데이터셋
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06942966B1

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