HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660563Generated: October 29, 2026
Boron tribromide → HCID 57777394, compound
https://huagongshe.com/reaction/660563
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 68839778 | HCID 68839778 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57777394 | HCID 57777394 | — |
Reaction Steps
To a solution of (S)-3-[3-benzyloxy-4-(1,1,4-trioxo-1,2,5-thiadiazolidin-2-yl)-benzyl]-2,3-dihydrobenzo[c]azepin-1-one in methylene chloride (2 mL) at −10° C. is added 0.3 mL of BBr3. The mixture is stirred at −10° C. for 30 min and is quenched with water. The aqueous phase is separated and lyophilized to give the title compound: 1H NMR (DMSO-d6) δ 9.61 (br s, 1H), 8.30 (d, J=5.56 Hz, 1H), 7.84 (d, J=7.58 Hz, 1H), 7.52 (t, J=7.07 Hz, 1H), 7.40 (t, J=7.58 Hz, 1H), 7.32 (d, J=8.0 Hz, 1H), 7.24 (d, J=8.08 Hz, 1H), 6.71 (m, 3H), 6.17 (m, 1H), 4.30 (s, 2H), 3.64 (m, 1H), 2.68 (m, 1H), 2.77 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08084448B2 |
|---|
| Source dataset | uspto-grants-2011_12 |
|---|
| ORD ID | ord-dde1b0e14f12480ba21795e1ba4a84ea |
|---|
| Source note | uspto-grants-2011_12 |
|---|