Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | N1-(benzo[d]isothiazol-3-yl)ethane-1,2-diamine | HCID 16768374 | — |
| Reactant | N-(tert-Butoxycarbonyl)-N-phenylglycine | HCID 21905636 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11669078 | HCID 11669078 | 54.5% |
Reaction Steps
A mixture of N1-(benzo[d]isothiazol-3-yl)ethane-1,2-diamine (600 mg, 3.1 mmol), N α (t-butoxycarbonyl)phenylglycine (850 mg, 3.4 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (650 mg, 3.4 mmol), 1-hydroxybenzotriazole (520 mg, 3.4 mmol) and triethylamine (950 μL, 6.8 mmol) in dichloromethane (50 mL) was allowed to stir at room temperature overnight. The reaction mixture was washed successively with 1N aqueous hydrochloric acid, saturated sodium bicarbonate solution and water, then dried over anhydrous sodium sulfate, filtered and the filtrate concentrated under reduced pressure. Purification by flash column chromatography, on silica gel, eluting with a mixture of 30% ethyl acetate in hexanes and selected fractions were combined and concentrated under reduced pressure to give (S)-tert-butyl 2-(2-(benzo[d]isothiazol-3-ylamino)ethylamino)-2-oxo-1-phenylethylcarbamate (720 mg) as a white solid. 1H NMR (300 MHz, CDCl3): 7.78 (d, 1H), 7.61 (d, 1H), 7.49 (t, 1H), 7.30 (t, 1H), 7.21 (m, 2H), 7.18 (m, 2H), 6.95 (t, 1H), 5.66 (m, 2H), 5.10 (broad s, 1H), 3.62 (m, 4H), 1.39 ppm (s, 9H). MW=427 confirmed by LC-MS, tr=13.38 min (Method Y) MH+=428.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776847B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-b0ef1e469fa64f6ea0919fcbee0633b8 |
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| Source note | uspto-grants-2010_08 |
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