HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660328Generated: November 1, 2026
Dicyclohexylcarbodiimide → HCID 54402895, compound
https://huagongshe.com/reaction/1660328
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | (Z)-2-(2-Tritylaminothiazol-4-yl)-2-methoxyiminoacetic acid | HCID 2724510 | — |
| Reactant | HCID 15575766 | HCID 15575766 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 54402895 | HCID 54402895 | — |
Reaction Steps
N,N'-Dicyclohexylcarbodiimide (1.11 g) is added to a suspension, cooled to +4° C., of 2-methoxyimino-2-(2-tritylamino-thiazol-4-yl)-acetic acid, syn isomer (2.17 g) and 4-(2-tert.-butyoxycarbonylamino-ethyl)-5,6-dioxo-3-thioxo-perhydro-1,2,4-triazine (1.05 g) in ethyl acetate (50 cc). The mixture is stirred for 4 hours at 20° C., filtered and concentrated to dryness at 20° C. under 20 mm Hg (2.7 kPa). The residue is taken up in methylene chloride (20 cc) and the solution is poured into diisopropyl ether (250 cc). After filtration and drying, 4-(2-tert.-butoxycarbonylamino-ethyl)-5,6-dioxo-3-[2-methoxyimino-2-(2-tritylamino-thiazol-4-yl)-acetylthio]-1,4,5,6-tetrahydro-1,2,4-triazine (syn isomer) (0.73 g) is obtained in the form of a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04307116 |
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| Source dataset | uspto-grants-1981_12 |
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| ORD ID | ord-039e11bd1d714b868ebabe227f441cb0 |
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| Source note | uspto-grants-1981_12 |
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