HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904152Generated: October 31, 2026
Dicyclohexylcarbodiimide → HCID 131713478, compound
https://huagongshe.com/reaction/1904152
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 18820-83-2 | HCID 312731 | — |
| Reactant | HCID 12884459 | HCID 12884459 | — |
| Reactant | HCID 54498501 | HCID 54498501 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131713478 | HCID 131713478 | — |
Reaction Steps
A solution of 1 g of the product of Step A, 0.38 g of pyridine hydroiodide, 0.63 g of dicyclohexylcarbodiimide, 0.60 g of benzhydryl 3-acetoxymethyl-7-amino-ceph-3-eme-4-carboxylate and 5 ml of anhydrous dimethylformamide was stirred at room temperature for 30 minutes and was vacuum filtered to remove dicyclohexylurea. 100 ml of ether were added to the filtrate and the mixture was stirred for 10 minutes and was vacuum filtered. The product was rinsed with ether and was chromatographed over silica gel. Elution with a 7-1 ethyl acetate-ethanol mixture yielded 0.524 g of the syn isomer of benzhydryl 3-acetoxymethyl-7-[2-2tritylamino-4-thiazolyl)-2-(2-morpholinoethoxyimino)-acetamido]-ceph-3-eme-4-carboxylate hydroiodide melting at 167° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04439433 |
|---|
| Source dataset | uspto-grants-1984_03 |
|---|
| ORD ID | ord-31c3df6b5a46432d843d10570b5129a2 |
|---|
| Source note | uspto-grants-1984_03 |
|---|