HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065196Generated: October 30, 2026
Dicyclohexylcarbodiimide → HCID 131712713, compound
https://huagongshe.com/reaction/1065196
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 18820-83-2 | HCID 312731 | — |
| Reactant | HCID 12884459 | HCID 12884459 | — |
| Reactant | HCID 54174508 | HCID 54174508 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131712713 | HCID 131712713 | — |
Reaction Steps
A mixture of 1.69 g of the product of Step A, 0.685 g of pyridine hydroiodide, 1.16 g of benzhydryl 3-acetoxymethyl-7-amino-ceph-3-eme-4-carboxylate and 1.36 g of dicyclohexylcarbodiimide was admixed with 17 ml of dimethylformamide and the mixture was cooled to 16° C. for 30 minutes and was then vacuum filtered. 400 ml of ether were added to the filtrate and the mixture was stirred for 5 minutes and allowed to stand for one hour. The mixture was decanted and the gum was washed with ether and was added to 50 ml of ether. The mixture was kneaded until concretization and was vacuum filtered. The product was washed with ether and dried to obtain 1.92 of raw product which was chromatographed over silica gel. Elution with a 91-9 chloroform-acetonitrile mixture yielded 790 mg of amorphous syn isomer of benzhydryl 3-acetoxymethyl-7-[2-(2-tritylamino-4-thiazolyl)-2-(2-thiocyanatoethoxyimino)-acetamido]-ceph-3-eme-4-carboxylate
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04328225 |
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| Source dataset | uspto-grants-1982_05 |
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| ORD ID | ord-b122df6a29ac40df8fffce779d280384 |
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| Source note | uspto-grants-1982_05 |
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