HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180207Generated: October 31, 2026
Tribromoborane-methyl sulfide → HCID 18186390, compound
https://huagongshe.com/reaction/1180207
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tribromoborane-methyl sulfide | HCID 4181510 | — |
| Reactant | HCID 69524407 | HCID 69524407 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18186390 | HCID 18186390 | 71.3% |
Reaction Steps
To a solution of 1-({4-[6-(dimethylamino)(3-pyridyl)]phenyl}mehyl)-2-(4fluorophenyl)-6-(phenylmethoxy)-1,2,3,4-tetrahydroisoquinoline (0.58 g, 1.07 mmol) in anhydrous dichloromethane (10 mL) under nitrogen at room temperature was added 1.0 M solution of boron tribromide-methyl sulfide complex in dichloromethane dropwise. After stirring for 5 hours, the reaction was quenched with ice-water and extracted with ethyl acetate. The extracts were dried over magnesium sulfate, filtered, and concentrated. The residue was then purified by chromatography (SiO2, 30-50% ethyl acetate/hexane) to provide the title compound (0.346 g, 71% yield): 1H NMR (CDCl3) 8.42 (d, 1H), 7.69 (dd, 1H), 7.38 (m, 2H), 7.05 (d, 2H), 6.93 (m, 2H), 6.79 (m, 2H), 6.53-6.67 (m, 4H), 5.09 (br, 1H), 4.76 (t, 1H), 3.58 (m, 1H), 3.48 (m, 1H), 3.17 (m 1H), 3.13 (s, 6H), 2.92 (m, 2H), 2.07 (dt, 1H); ES-MS m/z 454 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07279489B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-c5465b5b1a7e43d899bedb7a6bbb9ed7 |
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| Source note | uspto-grants-2007_10 |
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