HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(4-bromophenyl)-2-(pyrrolidin-1-yl)acetamide → N-[4-(6-Methoxybenzo[b]thiophen-2-yl)phenyl]-alpha-(1-pyrrolidinyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(4-bromophenyl)-2-(pyrrolidin-1-yl)acetamide | HCID 1091709 | — |
| Reactant | (6-Methoxy-1-benzothiophen-2-yl)boronic acid | HCID 10560276 | — |
| Product | N-[4-(6-Methoxybenzo[b]thiophen-2-yl)phenyl]-alpha-(1-pyrrolidinyl)acetamide | HCID 21182885 | 97% |
Reaction Steps
By essentially following the procedures described in Example 1, Part B, the title compound was prepared in 97% yield from N-(4-bromophenyl)-α-(1-pyrrolidinyl)acetamide (Part B) and 6-methoxybenzo[b]thiophene-2-boronic acid (Example 1, Part A).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06265575B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-48d8eba55f2b49bb92d98d802b8a706f |
| Source note | uspto-grants-2001_07 |