HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 86601726, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 57592502 | HCID 57592502 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | HCID 86601726 | HCID 86601726 | — |
Reaction Steps
[8-(4-Bromo-benzenesulfonyl)3-methyl-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-dimethyl-amine (D28) (1.4 g, 3.4 mmol) was cooled to −78° C. in tetrahydrofuran (20 ml) under an argon atmosphere. n-Butyllithium (1.6 ml, 2.5M) was added dropwise and the mixture stirred for 2 mins. Dimethylformamide (300 mg) was added and the mixture allowed to warm to room temperature then saturated ammonium chloride solution (50 ml) was added and the product extracted with ethyl acetate (2×50 ml). The organic layer was evaporated and chromatography on silica eluting with 0-20% methanol/ethyl acetate afforded the subtitled compound. MH+ 373.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07504392B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-6a08549888914b82a2f82521f1f35637 |
| Source note | uspto-grants-2009_03 |