Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 66583483 | HCID 66583483 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 89765672 | HCID 89765672 | 99% |
Reaction Steps
To a stirred solution of 3-chloro-4-(1-methyl-4,5-dihydro-1H-imidazol-2-ylsulfanyl)-phenylamine (5.0 g, 21 mmol) and diisopropylethylamine (5.37 g, 41.6 mmol) in dry tetrahydrofuran at 0° C. under N2 inert atmosphere, thiophosgene (2.39 g, 21 mmol) in tetrahydrofuran was added dropwise and stirred for 20 minutes. When the reaction was completed, the reaction mixture was concentrated at room temperature and taken in dichloromethane (100 mL), washed with water (2×50 mL) and dried over anhydrous MgSO4 to get the product as a brown solid (5.8 g, 99%). TLC: pet ether/ethyl acetate (8/2) Rf-0.4. LCMS (method A): mass found (M+H+, 282.0), Rt (min): 3.43, area % 71.5 (max); 1H NMR (400 MHz, DMSO-d6): δ 7.72 (d, J=2.16 Hz, 1H), 7.57 (s, 1H), 7.31 (m, 1H), 7.28 (m, 1H), 6.43 (d, J=8.56 Hz, 1H), 3.61 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09023851B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-9ee9f885743748108fdaa1abab905ade |
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| Source note | uspto-grants-2015_05 |
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