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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetic Anhydride → HCID 20246370, 화합물

HRID 1589545
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HRID 1589545 반응식
[NH2:1][C:2]1[N:7]=[C:6]2[N:8]=[CH:9][CH:10]=[C:5]2[C:4](=[O:11])[N:3]=1.[C:12](OC(=O)C)(=[O:14])[CH3:13]>N1C=CC=CC=1>[NH:1]([C:2]1[N:7]=[C:6]2[N:8]=[CH:9][CH:10]=[C:5]2[C:4](=[O:11])[N:3]=1)[C:12]([CH3:13])=[O:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 219043482-Amino-4H-pyrrolo[2,3-d]pyrimidin-4-one

생성물 1

HCID 20246370HCID 20246370, 화합물수율 64.9%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

2-Aminopyrrolo(2,3-d)pyrimidin-4-one (3.0 g) and acetic anhydride (10 g) are suspended in pyridine (50 ml) and the reaction is conducted under reflux for 24 hours. The solvent and excess reagent are distilled off under reduced pressure and, on an ice bath, 5% (W/V) alcoholic ammonia (20 ml) is added to the residue. The mixture is stirred for 2 hours. The resulting crystalline precipitate is collected by filtration and washed with dilute hydrochloric acid and water to give the above-identified compound (2.5 g).

후처리

  1. temperatureunder reflux for 24 hours
  2. distillationThe solvent and excess reagent are distilled off under reduced pressure and, on an ice bath
  3. addition5% (W/V) alcoholic ammonia (20 ml) is added to the residue
  4. filtrationThe resulting crystalline precipitate is collected by filtration
  5. washwashed with dilute hydrochloric acid and water

출처 및 근거

ORD 기록
ord-7121e7973161421b9de70abbaca75120
출처 데이터셋
uspto-grants-1986_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04571423

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