HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912689Generated: October 31, 2026
Benzoyl isothiocyanate → HCID 86631131, compound
https://huagongshe.com/reaction/912689
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl isothiocyanate | HCID 68284 | — |
| Reactant | 5-Aminomethyl-3-isopropylisoxazole | HCID 6483898 | — |
| Solvent | Ammonia | HCID 222 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86631131 | HCID 86631131 | 91.9% |
Reaction Steps
The title compound was prepared in accordance with the general method described in Example 12(a) by using 1-(3-isopropyl-isoxazol-5-yl)methylamine (0.85 g, 6.06 mmol), benzoyl isothiocyanate (0.90 mL, 6.67 mmol) and ammonia in methanol (7 N, 30 mL) with the exception that the reaction time for amine with benzoyl isothiocyanate was 12 h and the reaction mixture in ammonia was stirred o.n. Work-up was done by concentrating the reaction mixture in vacuo and adding ethyl acetate (15 mL) and water (15 mL). The is organic layer was separated, dried over sodium sulfate, filtered and concentrated. The residue was triturated with diethyl ether (10 mL) and the solid was removed by filtration. The filtrate was concentrated in vacuo to give the title compound (1.11 g, 91% yield), which was used in the next step without further purification. MS (ESI) m/z 200 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08026244B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-5242b3d5e8a94403bfa7e8efd760af4c |
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| Source note | uspto-grants-2011_09 |
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