HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrolidine → HCID 22493321, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 5-Bromoisatoic Anhydride | HCID 288561 | — |
| Reactant | HCID 22493358 | HCID 22493358 | — |
| Product | HCID 22493321 | HCID 22493321 | — |
Reaction Steps
{2-amino-5-bromophenyl}(1-pyrrolidinyl)methanone (prepared from pyrrolidine and 6-bromo-2H-3,1-benzoxazine-2,4(1H)-dione using the methods described in Example 17) and CMI were reacted using conditions described in the general procedure for CMI coupling to give {5-bromo-2-[(4,5-dihydro-1H-imidazol-2-ylmethyl)amino]phenyl}(1-pyrrolidinyl)methanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06884801B1 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-f16db3862e974e2f8f1bd1a88b88d810 |
| Source note | uspto-grants-2005_04 |