HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861897Generated: November 1, 2026
Ammonia → N-(1-methyl-1-(3-thioureidophenyl)ethyl)carbamic acid t-butyl ester
https://huagongshe.com/reaction/1861897
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | Calcium Carbonate | HCID 10112 | — |
| Reactant | 3-[2-(Boc-amino)-2-propyl]aniline | HCID 22981090 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(1-methyl-1-(3-thioureidophenyl)ethyl)carbamic acid t-butyl ester | HCID 22981132 | 89% |
Reaction Steps
Thiophosgene (0.12 ml) and a solution of the compound (284 mg) obtained in Example 2 in methylene chloride (10 ml) were added dropwise to a suspension of calcium carbonate (319 mg) in water (5 ml) at room temperature and stirred at room temperature for 5 h; thereafter, a 28% aqueous ammonia solution (5 ml) was added to the reaction mixture and stirred at room temperature for 16 h. After neutralization with 2 N HCl, the reaction mixture was extracted with ethyl acetate and the organic layer was washed with a saturated aqueous sodium chloride solution, dried with anhydrous sodium sulfate and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent, n-hexane:ethyl acetate=6:4) to yield 351 mg of the titled compound (yield, 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06534546B1 |
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| Source dataset | uspto-grants-2003_03 |
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| ORD ID | ord-39e09d5a2fc84f0baf78893282d6b565 |
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| Source note | uspto-grants-2003_03 |
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