HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Acetamide, N-(trimethylsilyl)- → Benzhydryl 7beta-[2-(2-tritylaminothiazol-4-yl)-2-difluoromethoxyiminoacetamido]-3-chloromethyl-3-cephem-4-carboxylate

HRID 1088041
Notes
Print preview

Reaction equation

HRID 1088041 reaction equation
[C:1]([NH:20][C:21]1[S:22][CH:23]=[C:24]([C:26](=[N:30][O:31][CH:32]([F:34])[F:33])[C:27](O)=[O:28])[N:25]=1)([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(C(C)C)CC)(C)C.S(Cl)(C)(=O)=O.[NH2:49][C@@H:50]1[C:75](=[O:76])[N:52]2[C:53]([C:59]([O:61][CH:62]([C:69]3[CH:74]=[CH:73][CH:72]=[CH:71][CH:70]=3)[C:63]3[CH:68]=[CH:67][CH:66]=[CH:65][CH:64]=3)=[O:60])=[C:54]([CH2:57][Cl:58])[CH2:55][S:56][C@H:51]12.C[Si](C)(C)NC(=O)C>CN(C)C=O.C(Cl)Cl.O>[C:1]([NH:20][C:21]1[S:22][CH:23]=[C:24]([C:26](=[N:30][O:31][CH:32]([F:33])[F:34])[C:27]([NH:49][C@@H:50]2[C:75](=[O:76])[N:52]3[C:53]([C:59]([O:61][CH:62]([C:63]4[CH:68]=[CH:67][CH:66]=[CH:65][CH:64]=4)[C:69]4[CH:70]=[CH:71][CH:72]=[CH:73][CH:74]=4)=[O:60])=[C:54]([CH2:57][Cl:58])[CH2:55][S:56][C@H:51]23)=[O:28])[N:25]=1)([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

9

Reactant 5

HCID 25989Acetamide, N-(trimethylsilyl)-HCID 31297Methanesulfonyl chlorideHCID 81531DiisopropylethylamineHCID 11236306(6R,7R)-benzhydryl 7-amino-3-(chloromethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylateHCID 536668022-(2-Tritylamino-4-thiazolyl)-2-difluoromethoxyimino-acetic acid

Product 1

HCID 131716601
Benzhydryl 7beta-[2-(2-tritylaminothiazol-4-yl)-2-difluoromethoxyiminoacetamido]-3-chloromethyl-3-cephem-4-carboxylate
Yield 105.8%

Reagents, catalysts & solvents 3

HCID 962WaterSolventHCID 6228DimethylformamideSolventHCID 6344DichloromethaneSolvent

Conditions

Temperature
-30 °C

Procedure

A mixture of 2-(2-tritylaminothiazol-4-yl)-2-difluoromethoxyiminoacetic acid (syn isomer) (2.4 g) and diisopropylethylamine (1.29 g) in N,N-dimethylformamide (35 ml) was cooled to -30° C. and mesyl chloride (1.15 g) was added dropwise thereto. The mixture was stirred at -20° to -30° C. for 30 minutes to give an activated acid solution. On the other hand, a mixture of benzhydryl 7β-amino-3-chloromethyl-3-cephem-4-carboxylate (2.18 g) and N-trimethylsilylacetamide (5.25 g) in methylene chloride (20 ml) was stirred to be a clear solution for 30 minutes at room temperature and then cooled to -20° C. To this solution was added the activated acid solution obtained above in one portion. The mixture was stirred for 30 minutes at -15° to -10° C., poured into water and extracted with ethyl acetate. The extract was washed with water three times, dried over magnesium sulfate and evaporated under reduced pressure. The residue was triturated in diisopropyl ether to give benzhydryl 7β-[2-(2-tritylaminothiazol-4-yl)-2-difluoromethoxyiminoacetamido]-3-chloromethyl-3-cephem-4-carboxylate (syn isomer) (4.64 g).

Workup

  1. customto give an activated acid solution
  2. stirringwas stirred
  3. customfor 30 minutes
  4. customat room temperature
  5. temperaturecooled to -20° C
  6. additionTo this solution was added the activated acid solution
  7. customobtained above in one portion
  8. stirringThe mixture was stirred for 30 minutes at -15° to -10° C.
  9. extractionextracted with ethyl acetate
  10. washThe extract was washed with water three times
  11. dry with materialdried over magnesium sulfate
  12. customevaporated under reduced pressure
  13. customThe residue was triturated in diisopropyl ether

Sources & evidence

ORD record
ord-e160a36cf75141fc99b4ce8acbc4dc0a
Source dataset
uspto-grants-1990_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04960766

Reaction notes

Loading…

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes