HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Methylamino)-1-[4-(pyrrolidin-1-yl)phenyl]ethan-1-ol → 7-Oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-3-sulfonic acid [2-hydroxy-2-(4-pyrrolidine-1-yl-phenyl)-ethyl]-methyl-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Methylamino)-1-[4-(pyrrolidin-1-yl)phenyl]ethan-1-ol | HCID 21098586 | — |
| Reactant | 7-Oxo-4,5,6,7-tetrahydrobenzo[b]thiophene-3-sulfonyl chloride | HCID 21098685 | — |
| Product | 7-Oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-3-sulfonic acid [2-hydroxy-2-(4-pyrrolidine-1-yl-phenyl)-ethyl]-methyl-amide | HCID 21098681 | — |
Reaction Steps
From 2-methylamino-1-(4-pyrrolidine-1-yl-phenyl)-ethanol (the compound of Preparation Example 19) (63 mg) and 7-oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-3-sulfonyl chloride (the compound of Preparation Example 7) (70 mg), the title compound (35 mg) was obtained as a colorless amorphous substance, in the same way as Preparation Example 41.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07217723B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-cf226c6c24064da8b32a98d99d0d4e1f |
| Source note | uspto-grants-2007_05 |