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Ammonia → 4-Amino-2-chloro-5-iodo-6-methoxycarbonylpyrimidine

HRID 245277
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HRID 245277 반응식
[CH3:1][O:2][C:3]([C:5]1[C:10]([I:11])=[C:9](Cl)[N:8]=[C:7]([Cl:13])[N:6]=1)=[O:4].[NH3:14]>CS(C)=O>[CH3:1][O:2][C:3]([C:5]1[C:10]([I:11])=[C:9]([NH2:14])[N:8]=[C:7]([Cl:13])[N:6]=1)=[O:4]
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참가 물질

4

반응물 2

HCID 222Ammonia2회HCID 45588386Methyl 2,6-dichloro-5-iodopyrimidine-4-carboxylate

생성물 1

HCID 594321054-Amino-2-chloro-5-iodo-6-methoxycarbonylpyrimidine수율 89%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

2,6-Dichloro-5-iodopyrimidine-4-carboxylic acid methyl ester (12 g, 36 mmol) was dissolved in dry dimethyl sulfoxide (DMSO; 100 mL) and treated with a stream of ammonia at such a rate when combined with external water bath cooling to keep the temperature in the range of 20-30° C. After 90 min, the ammonia addition was complete and excess ammonia was removed from the mixture by sparging with a stream of nitrogen for 20 min. The mixture was poured into water (200 mL) with stirring and the precipitated product was extracted with ethyl acetate (75 mL) twice. The combined ethyl acetate extracts were washed twice with water (50 mL), once with saturated NaCl solution, dried and evaporated to give the title compound (10 g, 89% yield) that was used without further purification. MS: M/Z=313.

후처리

  1. customcombined with external water bath
  2. temperaturecooling
  3. customin the range of 20-30° C
  4. customexcess ammonia was removed from the mixture
  5. customby sparging with a stream of nitrogen for 20 min
  6. additionThe mixture was poured into water (200 mL)
  7. extractionthe precipitated product was extracted with ethyl acetate (75 mL) twice
  8. washThe combined ethyl acetate extracts were washed twice with water (50 mL), once with saturated NaCl solution
  9. customdried
  10. customevaporated

출처 및 근거

ORD 기록
ord-c661f75cb4d349ebbd37acb4d8de245c
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08658791B2

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