Hydrochloric Acid → Cni H1594

HRID 53615

반응식

HRID 53615 반응식
[NH2:1][C:2]1[CH:3]=[C:4]([C:8](=[O:10])[CH3:9])[CH:5]=[CH:6][CH:7]=1.[NH2:11][C:12]1[N:17]=[C:16](Cl)[CH:15]=[C:14]([CH3:19])[N:13]=1.Cl.[OH-].[K+]>O>[C:8]([C:4]1[CH:3]=[C:2]([NH:1][C:16]2[CH:15]=[C:14]([CH3:19])[N:13]=[C:12]([NH2:11])[N:17]=2)[CH:7]=[CH:6][CH:5]=1)(=[O:10])[CH3:9]

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 74173'-AminoacetophenoneHCID 14797Potassium HydroxideHCID 218102-Amino-4-chloro-6-methylpyrimidine

생성물 1

HCID 133110Cni H1594수율 78.5%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Compound No. 15: A suspension of m-aminoacetophenone (2.7 g) and 2-amino-4-chloro-6-methylpyrimidine (2.87 g) in 40 mL water was treated with 1.7 mL concentrated HCl and heated at reflux for 1 hour. Addition of 40 mL 1N KOH gave a light buff solid, which was filtered out and dried to give 3.8 g 4-(3-acetylphenyl)amino-2-amino-6-methylpyrimidine, mp 196°-98° C.

후처리

  1. temperatureheated
  2. temperatureat reflux for 1 hour
  3. customgave a light buff solid, which
  4. filtrationwas filtered out
  5. customdried

출처 및 근거

ORD 기록
ord-57b6db78e12649efb92bda60463822eb
출처 데이터셋
uspto-grants-1997_04
특허 번호
US05620983

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