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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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tert-Butanol → HCID 136181547, 화합물

HRID 848717
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HRID 848717 반응식
[P:1]([O:5][C@@H:6]1[C@@H:10]([CH2:11][OH:12])[O:9][C@@H:8]([N:13]2[C:23]3[N:22]=[C:20]([NH2:21])[NH:19][C:17](=[O:18])[C:16]=3[N:15]=[CH:14]2)[C@@H:7]1[OH:24])(O)([OH:3])=[O:2].C(O)(C)(C)C.C1([N:36]=C=NC2CCCCC2)CCCCC1>O.N.C(N)=O>[P:1]([O:5][C@@H:6]1[C@@H:10]([CH2:11][OH:12])[O:9][C@@H:8]([N:13]2[C:23]3[N:22]=[C:20]([NH2:21])[NH:19][C:17](=[O:18])[C:16]=3[N:15]=[CH:14]2)[C@@H:7]1[OH:24])([NH2:36])(=[O:2])[OH:3]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 6386tert-ButanolHCID 10868DicyclohexylcarbodiimideHCID 1353987273'-Gmp

생성물 1

HCID 136181547HCID 136181547, 화합물수율 50%

시약·촉매·용매 2

HCID 713Formamide용매HCID 12896473Azane;hydrate용매

반응 조건

온도
80 °C

실험 절차

Three millimoles of guanosine-3'-monophosphate were dissolved in a mixture of 7.5 ml of 2 N ammonia water and 5 ml of formamide, the solution was combined with 20 ml of tertiary butanol that contained 15 millimoles of dicyclohexyl carbodiimide, and the resulting mixture was heated at 80° C. for a period of 9 to 10 hours with care taken to prevent evaporation of the solvent. After the reaction, the mixture was left to stand overnight at room temperature, the precipitate was filtered off, the filtrate was concentrated under vacuum to remove the tertiary butanol, and the residue was extracted with ether. The aqueous layer was recovered, concentrated under vacuum, and the residue was treated with acetone to give a crystal of guanosine-3'-monophosphoramidate in a yield of about 50%. The crystal was heated under vacuum at 100° C. for a period of 3 to 4 hours until it was dehydrated thoroughly.

후처리

  1. customevaporation of the solvent
  2. customAfter the reaction
  3. waitthe mixture was left
  4. filtrationthe precipitate was filtered off
  5. concentrationthe filtrate was concentrated under vacuum
  6. customto remove the tertiary butanol
  7. extractionthe residue was extracted with ether
  8. customThe aqueous layer was recovered
  9. concentrationconcentrated under vacuum
  10. additionthe residue was treated with acetone

출처 및 근거

ORD 기록
ord-5b8ab559fab44be59b1a9b64a6a36ec8
출처 데이터셋
uspto-grants-1981_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04297347

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