HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638844Generated: October 31, 2026
N,N-Dimethylaniline → HCID 131716196, compound
https://huagongshe.com/reaction/1638844
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Benzhydryl 7-Amino-3-chloromethyl-3-cephem-4-carboxylate | HCID 13239626 | — |
| Reactant | HCID 53785634 | HCID 53785634 | — |
| Product | HCID 131716196 | HCID 131716196 | — |
Reaction Steps
1.0 g (1.4 mmol) of 2-[3,4-di(2-methoxyethoxymethoxy)benzyloxyimino]-2-(2-tritylaminothiazol-4-yl)acetic acid (syn-isomer) and 0.56 g (1.4 mmol) of benzhydryl 7-amino-3-chloromethyl-3-cephem-4-carboxylate were dissolved in 0.77 ml (6.3 mmol) of N,N-dimethylaniline at 0° C., and 0.12 ml (1.7 mmol) of phosphorus oxychloride was dropwise added thereto. The mixture was stirred for 30 minutes and the reaction solution was washed with sequentially with 1N hydrochloric acid, a 10% sodium hydrogencarbonate aqueous solution and a saturated sodium chloride aqueous solution. The water layer was further extracted with ethyl acetate, and the organic layer was added thereto. After drying over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure to obtain benzhydryl 3-chloromethyl-7-{2-[3,4-di(2-methoxyethoxymethoxy)benzyloxyimino]-2-(2-tritylaminothiazol-4-yl)acetamido}-3-cephem-4-carboxylate (syn-isomer), which was used for the next reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04880797 |
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| Source dataset | uspto-grants-1989_11 |
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| ORD ID | ord-4ffde1298d8340cb8c0cd51b9f1b450d |
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| Source note | uspto-grants-1989_11 |
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