HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1659421Generated: October 29, 2026
HCID 131712572, compound → HCID 131712571, compound
https://huagongshe.com/reaction/1659421
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 131712572 | HCID 131712572 | — |
| Reactant | HCID 178447172 | HCID 178447172 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | HCID 131712571 | HCID 131712571 | — |
Reaction Steps
A mixture of 3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-7-[2-(2-tert-pentyloxycarbonylamino-1,3-thiazol-4-yl)glyoxylamido]-3-cephem-4-carboxylic acid, which can be represented as 3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-7-[2-(2-tert-pentyloxycarbonylimino-2,3-dihydro-1,3-thiazol-4yl)glyoxylamido]-3-cephem-4-carboxylic acid, (1.8 g.) and 98 to 100% formic acid (40 ml.) was allowed to stand for 5 hours. After the reaction, the reaction mixture was post-treated in the similar manners as in Examples 16 to 17 to give 3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-7-[2-(2-amino-1,3-thiazol-4-yl)glyoxylamido]-3-cephem-4-carboxylic acid, which can be represented as 3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-7-[2-(2-imino-2,3-dihydro-1,3-thiazol-4-yl)glyoxylamido]-3-cephem-4-carboxylic acid, (0.32 g.), mp. 147° to 160° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04303655 |
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| Source dataset | uspto-grants-1981_12 |
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| ORD ID | ord-bb743de9cfa54d48a5e311dd4e4e68f2 |
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| Source note | uspto-grants-1981_12 |
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