HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460635Generated: October 29, 2026
Boron tribromide → HCID 22728961, compound
https://huagongshe.com/reaction/460635
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 22729047 | HCID 22729047 | — |
| Product | HCID 22728961 | HCID 22728961 | 78.6% |
Reaction Steps
By the reactions in the same manner as in Starting Material Synthesis Example 5 using 4-(4-methoxybenzo(b)furan-2-yl)-2-methylthiazole (2.7 g) obtained in Starting Material Synthesis Example 67 and boron tribromide (7.5 g), 4-(4-hydroxybenzo(b)furan-2-yl)-2-methylthiazole (2.0 g) was obtained as yellow crystals. By the reactions in the same manner as in Starting Material Synthesis Example 2 using this compound, (S)-glycidyl nosylate (2.9 g) and potassium carbonate (3.1 g), (S)-4-(4-glycidyloxybenzo(b)furan-2-yl)-2-methylthiazole (2.1 g) was obtained as a brown oil. By the reactions in the same manner as in Example 1 using the brown oil and 4-(naphthalen-2-yl)piperidine (1.5 g), the title compound (0.3 g) was obtained as white crystals, melting point 148–150° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07196199B2 |
|---|
| Source dataset | uspto-grants-2007_03 |
|---|
| ORD ID | ord-03d9428db5464b87b5aadb451c57fbdb |
|---|
| Source note | uspto-grants-2007_03 |
|---|