HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031207Generated: October 30, 2026
Anisole → (Z)-2-((((5-Amino-1,2,4-thiadiazol-3-yl)(carboxy)methylene)amino)oxy)-2-methylpropanoic acid
https://huagongshe.com/reaction/1031207
Participants
| Role | Name | HCID | Charge |
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| Reactant | Anisole | HCID 7519 | — |
| Reactant | (2Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(2-methyl-1-((2-methylpropan-2-yl)oxy)-1-oxopropan-2-yl)oxyiminoacetic acid | HCID 13577059 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | (Z)-2-((((5-Amino-1,2,4-thiadiazol-3-yl)(carboxy)methylene)amino)oxy)-2-methylpropanoic acid | HCID 15077653 | 88% |
Reaction Steps
A solution of (Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(1-tert-butoxycarbonyl-1-methylethoxyimino)acetic acid (17.8 g) and anisole (18 ml) in trifluoroacetic acid (36 ml) was stirred for 4.0 hours at room temperature. The reaction mixture was concentrated under reduced pressure and an aqueous solution of sodium bicarbonate was added thereto to adjust to pH 6.0. The aqueous solution was washed with ethyl acetate, adjusted to pH 3.8 with 6N hydrochloric acid and washed with ethyl acetate. The aqueous layer was separated and 6N hydrochloric acid was added thereto to adjust to pH 1.0. After the mixture was stirred for 10 minutes, the resultant precipitate was collected by filtration to give (Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(1-carboxy-1-methylethoxyimino)acetic acid (13.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05108997 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-2a8631dde28340aebda15b4881367c39 |
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| Source note | uspto-grants-1992_04 |
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