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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → HCID 178518410, 화합물

HRID 1365128
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HRID 1365128 반응식
[NH:1]([C:5]1[CH:9]=[CH:8][O:7][C:6]=1[C:10]([O:12]CC)=O)[C:2]([NH2:4])=[O:3].[OH-].[Na+].Cl>CO>[N:1]1[C:5]2[CH:9]=[CH:8][O:7][C:6]=2[C:10]([OH:12])=[N:4][C:2]=1[OH:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 59593138Ethyl 3-ureidofuran-2-carboxylate

생성물 1

HCID 178518410HCID 178518410, 화합물수율 97.7%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Ethyl 3-ureidofuran-2-carboxylate 35 (120 mg, 1.0 eq) was suspended in methanol (6 ml) and treated with 1.5 M NaOH (1.5 ml). Reaction mixture was heated to reflux for 90 minutes. Reaction mixture was allowed to cool down to room temperature, and was acidified with 6N HCl up to pH 3. Mixture was concentrated. Methanol was added to residue and solid was filtered and dried at 95° C. under high vacuum for 24 h to yield furo[3,2-d]pyrimidine-2,4-diol 36 (90 mg, 91%) which was used in the next reaction without further purification.

후처리

  1. customReaction mixture
  2. temperaturewas heated
  3. temperatureto reflux for 90 minutes
  4. customReaction mixture
  5. concentrationMixture was concentrated
  6. additionMethanol was added to residue and solid
  7. filtrationwas filtered
  8. customdried at 95° C. under high vacuum for 24 h

출처 및 근거

ORD 기록
ord-e5b445e07d2d40e1b977b08607a48c76
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07888352B2

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