HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 54519295, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 54182443 | HCID 54182443 | — |
| Reactant | 2-(5-Chlorothiophen-2-yl)ethenesulfonyl chloride | HCID 54463064 | — |
| Reactant | HCID 69028555 | HCID 69028555 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54519295 | HCID 54519295 | — |
Reaction Steps
Sodium borohydride (0.005 g, 0.13 mmol) is added to a solution of 2-{4-[2-(5-chloro-thiophen-2-yl)-ethenesulfonyl]-2-(±)-methoxycarbonyl-6-oxo-piperazin-1-ylmethyl}-pyrrolo[3,2-c]pyridine-1-carboxylic acid tert-butyl ester (0.04 g, 0.07 mmol), (prepared from 2-(2-(±)-methoxycarbonyl-6-oxo-piperazin-1-ylmethyl)-pyrrolo[3,2-c]pyridine-1-carboxylic acid tert-butyl ester, EXAMPLE 71, and 2-(5-chloro-thiophen-2-yl)-ethenesulfonyl chloride, EXAMPLE 3, using the procedure described in EXAMPLE 214, Part A) in MeOH (3 mL) at RT. The reaction mixture is stirred for 6 h then quenched with water and concentrated in vacuo. The crude product (0.04 g) is taken onto the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07612075B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-bee0f9d895c041f8850757b9cd95aef4 |
| Source note | uspto-grants-2009_11 |