HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236313Generated: October 29, 2026
Dichloromethane → HCID 178512708, compound
https://huagongshe.com/reaction/236313
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,2'-Thiobis(1H-isoindole-1,3(2H)-dione) | HCID 82196 | — |
| Reactant | HCID 178478604 | HCID 178478604 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 178512708 | HCID 178512708 | 54% |
Reaction Steps
A mixture of crude N-{2-[(2-guanidinothiazol-4-yl)methylthio]ethyl}ethanediimidamide trihydrochloride (5.65 g, 13.7 mmoles) [prepared in Step A], 50 ml of CH2Cl2 and 5.7 ml of triethylamine was treated with N,N'-thiobisphthalimide (DMF solvate) (5.44 g; 13.7 mmoles) and stirred for one hour to give a thick suspension. The mixture was treated with 40 ml of 2N NaOH and the solvents were decanted from the gum-like material which had separated. The gum was washed with 40 ml of 2N NaOH, water, and then dissolved in methanol and concentrated to give 3.0 g of crude product. The product was purified by flash chromatography on 90 g of silica gel (230-400 mesh) using ethyl acetate-methanol (97:3) as the eluent to give 2.44 g (54%) of the title compound. Treatment of the product in 35 ml of acetone with one equivalent of cyclohexylsulfamic acid gave the salt which was then recrystallized from 95 % aqueous ethanol to give the title compound as its cyclohexylsulfamate salt, mp. 171°-173.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04644006 |
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| Source dataset | uspto-grants-1987_02 |
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| ORD ID | ord-9271a862ddf648679bd9597e71b2d674 |
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| Source note | uspto-grants-1987_02 |
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