HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895980Generated: October 30, 2026
Diethyl Ether → 2-Naphthalen-2-ylmethyl-1-(11-oxo-10,11-dihydro-5H-dibenzo[b,e][1,4]diazepin-2-yl)-isothiourea
https://huagongshe.com/reaction/895980
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 2-Bromomethylnaphthalene | HCID 70320 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (11-Oxo-10,11-dihydro-5H-dibenzo[b,e][1,4]diazepin-2-yl)-thiourea | HCID 11300593 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Naphthalen-2-ylmethyl-1-(11-oxo-10,11-dihydro-5H-dibenzo[b,e][1,4]diazepin-2-yl)-isothiourea | HCID 178511890 | — |
Reaction Steps
To a stirred solution of (11-oxo-10,11-dihydro-5H-dibenzo[b,e][1,4]diazepin-2-yl)-thiourea (Example 9, 50 mg, 0.18 mmol) in DMF (1 mL) was added 2-bromomethylnaphthalene (38.8 mg, 0.18 mmol) in one portion. The reaction mixture was stirred at room temperature for 1 hr then heated at 60° C. for 2 hrs. After this time, the solvent was removed in vacuo to leave an oily residue which was triturated with diethyl ether to give a yellow-brown solid. The solid was dissolved in 5 mL of tetrahydrofuran: 5 mL diethyl ether and treated with saturated sodium bicarbonate (10 mL). The organic layer was separated, dried over magnesium sulfate and evaporated to give a yellow oil. The product was purified by chromatography on silica gel (2% methanol: 98% dichloromethane). H1 NMR (acetone d6) δ: 8.81 (bs, 1H), 7.92-7.85 (m, 4H), 7.61 (bs, 1H), 7.50-7.39 (m, 4H), 7.09-6.91 (m, 7H), 5.81 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06919328B1 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-cb656248c9fe4c25b2456862cfa809d8 |
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| Source note | uspto-grants-2005_07 |
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