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Hydrochloric Acid → HCID 135741792, 화합물

HRID 1022425
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HRID 1022425 반응식
[Cl:1][C:2]1[N:3]=[C:4](Cl)[C:5]2[CH:10]=[CH:9][N:8]([CH3:11])[C:6]=2[N:7]=1.[OH-:13].[K+].Cl>>[Cl:1][C:2]1[NH:3][C:4](=[O:13])[C:5]2[CH:10]=[CH:9][N:8]([CH3:11])[C:6]=2[N:7]=1
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참가 물질

4

반응물 3

HCID 313Hydrochloric AcidHCID 14797Potassium HydroxideHCID 252309532,4-Dichloro-7-methyl-7H-pyrrolo[2,3-d]pyrimidine

생성물 1

HCID 135741792HCID 135741792, 화합물수율 100.6%

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온도
100 °C

실험 절차

2,4-dichloro-7-methyl-7H-pyrrolo[2,3-d]pyrimidine (2.39 g, 11.8 mmol) was treated with a 2M aqueous potassium hydroxide solution (70 mL, 140 mmol). The reaction was warmed to 100° C., where it was stirred overnight. The reaction was allowed to cool down to room temperature gradually, where it stirred for an additional 2 nights. The reaction was brought to pH ˜7-8 with a 3N aqueous hydrochloric acid solution. The resulting light yellow mixture was cooled in an ice/water bath and filtered, rinsing twice with a small amount of water. The filtrate was brought to pH ˜2-3 with additional 3N aqueous hydrochloric acid solution. The resulting opaque light yellow mixture was filtered through the original filter cake. The solids were dried in vacuo to afford 2-chloro-7-methyl-3,7-dihydro-pyrrolo[2,3-d]pyrimidin-4-one as an off-white solid (2.18 g, 100%). NMR (300 MHz, DMSO-d6) δ ppm 3.67 (s, 3H) 6.46 (d, J=3.39 Hz, 1H) 7.11 (d, J=3.39 Hz, 1H) 12.83 (br. s., 1H). LC-MS calcd. for C7H7ClN3O [(M+H)+] 184, obsd, 183.9.

후처리

  1. temperatureto cool down to room temperature gradually
  2. stirringwhere it stirred for an additional 2 nights
  3. temperatureThe resulting light yellow mixture was cooled in an ice/water bath
  4. filtrationfiltered
  5. washrinsing twice with a small amount of water
  6. filtrationThe resulting opaque light yellow mixture was filtered through the original filter cake
  7. customThe solids were dried in vacuo

출처 및 근거

ORD 기록
ord-754112e1d90a4c8ab0737fe544d130fb
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08722661B2

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