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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → HCID 20525070, 화합물

HRID 1702794
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HRID 1702794 반응식
[ClH:1].C(OC([NH:9][CH2:10][CH2:11][CH2:12][NH:13][C:14]([N:16]1[CH:23]=[C:22]([F:24])[C:20](=[O:21])[NH:19][C:17]1=[O:18])=[O:15])=O)(C)(C)C>C(O)C>[ClH:1].[NH2:9][CH2:10][CH2:11][CH2:12][NH:13][C:14]([N:16]1[CH:23]=[C:22]([F:24])[C:20](=[O:21])[NH:19][C:17]1=[O:18])=[O:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 20525037HCID 20525037, 화합물

생성물 1

HCID 20525070HCID 20525070, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Hydrogen chloride gas was introduced to the solution of 1-[N-[3-(t-butoxycarbonylamino)propyl]carbamoyl]-5-fluorouracil (5.1 g.) which was prepared in Example 20 in ethanol (30 ml.) until precipitates were appeared for 1 hour with stirring under cooling with ice. The reaction mixture was further stirred for 1 hour at ambient temperature, and diethyl ether (100 ml.) was added therein. The resultant crystalline precipitates were collected by filtration and were dried over phosphoric anhydride to give 1-[N-(3-aminopropyl)carbamoyl]-5-fluorouracil hydrochloride (1.5 g.).

후처리

  1. customuntil precipitates
  2. temperatureunder cooling with ice
  3. stirringThe reaction mixture was further stirred for 1 hour at ambient temperature
  4. additiondiethyl ether (100 ml.) was added
  5. customThe resultant crystalline precipitates
  6. filtrationwere collected by filtration
  7. dry with materialwere dried over phosphoric anhydride

출처 및 근거

ORD 기록
ord-7d3ced70ccde4ad9858aa0392fd45052
출처 데이터셋
uspto-grants-1982_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04349552

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