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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4(3H)-Quinazolinone, 3-amino-2-hydrazino- → 3-amino-2-(4-hydroxybutylamino)-quinazolin-4(3H)-one

HRID 1702976
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반응식

HRID 1702976 반응식
[NH2:1][N:2]1[C:11](=[O:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[N:4]=[C:3]1[NH:13]N>NCCCCO>[NH2:1][N:2]1[C:11](=[O:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[N:4]=[C:3]1[NH:13][CH2:8][CH2:9][CH2:10][CH2:11][OH:12]
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참가 물질

3

반응물 1

HCID 640574(3H)-Quinazolinone, 3-amino-2-hydrazino-

생성물 1

HCID 129441293-amino-2-(4-hydroxybutylamino)-quinazolin-4(3H)-one수율 116%

시약·촉매·용매 1

HCID 258684-Amino-1-butanol용매

실험 절차

16 g of 3-amino-2-hydrazinoquinazolin-4(3H)-one were stirred in 48 ml of 4-aminobutanol at 160° C. for 3 days and the majority of the 4-aminobutanol was then distilled off under vacuum. The residue was diluted with water and the mixture was seeded and stored at 0° C. overnight to crystallize the product. The mixture was filtered and the recovered product was washed and dried to obtain 12.05 g of 3-amino-2-(4-hydroxybutylamino)-quinazolin-4(3H)-one.

후처리

  1. distillationthe majority of the 4-aminobutanol was then distilled off under vacuum
  2. additionThe residue was diluted with water
  3. customto crystallize the product
  4. filtrationThe mixture was filtered
  5. washthe recovered product was washed
  6. customdried

출처 및 근거

ORD 기록
ord-07af5b9f35ab44a8b67e8e3dfb7b95c0
출처 데이터셋
uspto-grants-1982_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04350695

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