HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345646Generated: October 29, 2026
Water → 4-Chloromethyl-3-[2-(2-tritylamino-4-thiazolyl)-2-trityloxyimino-acetamido]-2-oxo-azetidine
https://huagongshe.com/reaction/345646
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 4-Chloromethyl-3-amino-2-oxo-azetidine hydrochloride | HCID 19992113 | — |
| Reactant | Sodium 2-(2-tritylamino-4-thiazolyl)-2-trityloxyimino-acetic acid | HCID 86743756 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 4-Chloromethyl-3-[2-(2-tritylamino-4-thiazolyl)-2-trityloxyimino-acetamido]-2-oxo-azetidine | HCID 53647805 | — |
Reaction Steps
A mixture of 1.527 g of the syn isomer of sodium 2-(2-tritylamino-4-thiazolyl)-2-trityloxyimino-acetic acid, 419 mg of tosyl chloride and 15 ml of methylene chloride was stirred for 40 minutes and then a solution of 342 mg of 4-chloromethyl-3-amino-2-oxo-azetidine hydrochloride in 15 ml of methylene chloride and 0.6 ml of triethylamine was added thereto. The mixture was stirred for 2 hours and water was added thereto with stirring. The decanted aqueous phase was extracted with methylene chloride and the combined organic phases were dried, filtered and evaporated to dryness under reduced pressure. The residue was chromatographed over silica gel and was eluted with ether to obtain 736 mg of syn isomer of 4-chloromethyl-3-[2-(2-tritylamino-4-thiazolyl)-2-trityloxyimino-acetamido]-2-oxo-azetidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05057512 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-8bc9b9e7bcff4201a5d63c1aea5eff1e |
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| Source note | uspto-grants-1991_10 |
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