HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463941Generated: October 30, 2026
Dicyclohexylcarbodiimide → HCID 131712193, compound
https://huagongshe.com/reaction/463941
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | HCID 12882024 | HCID 12882024 | — |
| Reactant | 2-Methoxyimino-2-(1,2,3-thiadiazol-4-yl)acetic acid | HCID 54347340 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131712193 | HCID 131712193 | 64.1% |
Reaction Steps
Dicyclohexylcarbodiimide (0.99 g.) was added at ambient temperature to a solution of diphenylmethyl 7-amino-7-methoxy-3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylate (2.1 g.) in dry tetrahydrofuran (20 ml.) and then 2-methoxyimino-2-(1,2,3-thiadiazol-4-yl)acetic acid (syn isomer) (0.9 g) was added thereto at ambient temperature to give white precipitates. After stirring for 2 days at ambient temperature, the precipitates were filtered off and the filtrate was concentrated under reduced pressure to give brown oil. The oil as subjected to column chromatography on silica gel, eluted with a mixture of chloroform and ethyl acetate and the eluate was concentrated under reduced pressure to give diphenylmethyl 7-[2-methoxyimino-2-(1,2,3-thiadiazol-4-yl)acetamido]-7-methoxy-3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylate (syn isomer) (1.78 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04544751 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-1b0a1b11fa7348beac2c8686ebbaff4c |
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| Source note | uspto-grants-1985_10 |
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