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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432955Generated: November 2, 2026

Sodium borohydride → HCID 54519295, compound

https://huagongshe.com/reaction/1432955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 54182443HCID 54182443—
Reactant2-(5-Chlorothiophen-2-yl)ethenesulfonyl chlorideHCID 54463064—
ReactantHCID 69028555HCID 69028555—
SolventMethanolHCID 887—
ProductHCID 54519295HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612075B2
Source datasetuspto-grants-2009_11
ORD IDord-bee0f9d895c041f8850757b9cd95aef4
Source noteuspto-grants-2009_11