HuagongsheHuagongshe Chemistry Print Report · For research reference only
Anisole → 4-Bromoacetyl-7-methoxy-2-(4-methoxyphenyl)-2,3,4,5-tetrahydro-1,4-benzothiazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Anisole | HCID 7519 | — |
| Reactant | 4-Bromoacetyl-2-chloro-7-methoxy-2,3,4,5-tetrahydro-1,4-benzothiazepine | HCID 15291664 | — |
| Product | 4-Bromoacetyl-7-methoxy-2-(4-methoxyphenyl)-2,3,4,5-tetrahydro-1,4-benzothiazepine | HCID 15291665 | 74.3% |
Reaction Steps
The above-mentioned 4-bromoacetyl-2-chloro-7-methoxy-2,3,4,5-tetrahydro-1,4-benzothiazepine (0.19 g), anisole (0.07 g) end stannic chloride (0.17 g) were reacted in the same manner as in Experimental Example 13 to give 4-bromoacetyl-7-methoxy-2-(4-methoxyphenyl)-2,3,4,5-tetrahydro-1,4-benzothiazepine (0.17 g). This compound (0.1g), 4-benzyl piperidine (0.09 g) and potassium carbonate (0.11 g) were reacted in the same manner as in Experimental Example 6 to give 4-[1-(4-benzyl)piperidinyl]acetyl-7-methoxy-2-(4-methoxyphenyl)-2,3,4,5-tetrahydro-1,4-benzothiazepine (0.20 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05416066 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-a259f9fa12a74070bc9dfbd8763884b8 |
| Source note | uspto-grants-1995_05 |