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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1806391Generated: November 1, 2026

Pyrrolidine → HCID 57732730, compound

https://huagongshe.com/reaction/1806391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 66723400HCID 66723400—
ProductHCID 57732730HCID 57732730—

Reaction Steps

To 5-(5-acetyl-3-thienyl)-3-[1-(ethylsulfonyl)-4-piperidinyl]-1H-indole-7-carboxamide (10 mg, 0.02 mmol) was added sodium cyanoborohydride (7.5 mg, 0.12 mmol) and pyrrolidine (0.03 mL, 0.30 mmol). The resulting mixture was reacted in a microwave for 40 min at 150° C. All the solvent was evaporated and the crude product was partitioned between ethyl acetate (1.5 mL) and 1 M sodium hydroxide (0.2 mL). The reaction was purified by SFC to give the title compound as 100% chirally pure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354406B2
Source datasetuspto-grants-2013_01
ORD IDord-dfbf5762fff94c6db233087a31db8689
Source noteuspto-grants-2013_01