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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Diethyl Ether → Sodium

HRID 1414004
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HRID 1414004 반응식
FC(F)(F)C(O)=O.[O:8]=[C:9]1[N:16]2[CH:11]([S:12][CH2:13][CH:14]=[C:15]2[C:17]([OH:19])=[O:18])[CH2:10]1.C(OCC)(=O)CCCCC.[Na:30].C(OCC)C>CO.C(O)CCC>[O:8]=[C:9]1[N:16]2[CH:11]([S:12][CH2:13][CH:14]=[C:15]2[C:17]([OH:19])=[O:18])[CH2:10]1.[Na:30]
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참가 물질

7

반응물 3

HCID 3283Diethyl EtherHCID 53628222Sodium 2-ethyl hexanoateHCID 775092038-Oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, trifluoroacetate salt

생성물 2

HCID 5360545SodiumHCID 190919938-Oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

시약·촉매·용매 2

HCID 263
1-Butanol
용매
HCID 887Methanol용매

실험 절차

While stirring 0.8 g of [6R-[6α, 7β(Z)]]-3-[(Acetyloxy)methyl]-7-[[(2-amino-4-thiazolyl)[2-oxo-2-[(phenylmethoxy)amino]ethoxy]imino]acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, trifluoroacetate salt is dissolved in 5 ml methanol. At 0° C. an equivalent amount of sodium ethyl hexanoate in butanol is added while stirring. After 10 min. 100 ml of dry diethyl ether is added and the precipitate is filtered off to yield 0.69 g of [6R-[6α, 7β(Z)]]-3-[(Acetyloxy)methyl]-7-[[(2-amino-4-thiazolyl)[2-oxo-2-[(phenylmethoxy)amino]ethoxy]imino]acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, sodium salt having a melting point of 168° C. to 173° C.

후처리

  1. filtrationthe precipitate is filtered off

출처 및 근거

ORD 기록
ord-5cc0379f752d49f4993b606a5658b3b7
출처 데이터셋
uspto-grants-1981_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04252802

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