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Xanthine → 6-Thioxanthine

HRID 377183
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HRID 377183 반응식
[NH:1]1[C:10](=O)[C:9]2[NH:8][CH:7]=[N:6][C:5]=2[NH:4][C:2]1=[O:3].P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=[S:13].[OH-].[Na+]>N1C=CC=CC=1>[NH:1]1[C:10](=[S:13])[C:9]2[NH:8][CH:7]=[N:6][C:5]=2[NH:4][C:2]1=[O:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1188XanthineHCID 14798Sodium HydroxideHCID 14817Phosphorus sulfide (P2S5)

생성물 1

HCID 12681076-Thioxanthine수율 354.5%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

6.59 g (19 mM) of xanthine and 5.07 g (22.8 mM) of phosphorus pentasulfide were heated under reflux in 102 ml of pyridine for 3 days. At 0° C., 25.1 ml of 2N NaOH were added. The solid was filtered off and washed with pyridine. The solvents were evaporated in vacuo, the residue suspended in water, collected, redissolved in 100 ml of 1N NaOH and 50 ml of isopropanol, treated twice with 0.3 g of charcoal, filtered and neutralized with 5N HCl to pH 7. The isopropanol was removed in vacuo and the solid collected, washed and dried to give 6.80 g (98.7%) of 6-thioxanthine, mp 188-9° C.

후처리

  1. filtrationThe solid was filtered off
  2. washwashed with pyridine
  3. customThe solvents were evaporated in vacuo
  4. customcollected
  5. dissolutionredissolved in 100 ml of 1N NaOH
  6. addition50 ml of isopropanol, treated twice with 0.3 g of charcoal
  7. filtrationfiltered
  8. customThe isopropanol was removed in vacuo
  9. customthe solid collected
  10. washwashed
  11. customdried

출처 및 근거

ORD 기록
ord-5134e4564fc9476f8f4b10e279a89db2
출처 데이터셋
uspto-grants-2000_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06025361

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