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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → HCID 10513496, 화합물

HRID 2210434
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HRID 2210434 반응식
[CH:1]([NH:4][C:5]1[CH:10]=[CH:9][N:8]=[CH:7][C:6]=1[S:11]([NH2:14])(=[O:13])=[O:12])([CH3:3])[CH3:2].[CH2:15]=O.Cl>C(O)(C)C.C(OCC)(=O)C>[CH:1]([N:4]1[C:5]2[CH:10]=[CH:9][N:8]=[CH:7][C:6]=2[S:11](=[O:13])(=[O:12])[NH:14][CH2:15]1)([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 712FormaldehydeHCID 10632459HCID 10632459, 화합물

생성물 1

HCID 10513496HCID 10513496, 화합물

시약·촉매·용매 2

HCID 8857Ethyl Acetate촉매HCID 3776Isopropanol용매

실험 절차

A mixture of 1 g of 4-isopropylaminopyridine-3- sulfonamide (Preparation 3) and 1 g of paraformaldehyde in 20 cm3 of isopropanol to which 10 drops of ethyl acetate saturated with gaseous HCl have been added is brought to reflux for 3 hours. After cooling, the crystalline precipitate is filtered and washed with isopropanol. The precipitate is dissolved in 150 cm3 of hot methanol. The possible insoluble material is filtered. The filtrate is concentrated to dryness and the residue is taken up in 30 cm3 of water. The aqueous suspension is adjusted to a pH of 7-7.5 (NaHCO3) and the precipitate corresponding to the title compound is filtered, washed with water and dried.

후처리

  1. additionhave been added
  2. temperatureto reflux for 3 hours
  3. temperatureAfter cooling
  4. filtrationthe crystalline precipitate is filtered
  5. washwashed with isopropanol
  6. dissolutionThe precipitate is dissolved in 150 cm3 of hot methanol
  7. filtrationThe possible insoluble material is filtered
  8. concentrationThe filtrate is concentrated to dryness
  9. filtrationthe precipitate corresponding to the title compound is filtered
  10. washwashed with water
  11. customdried

출처 및 근거

ORD 기록
ord-7a8afa0d1438446ba6d7884e93c5a6d7
출처 데이터셋
uspto-grants-1995_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05459138

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