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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216632Generated: November 1, 2026

Sodium borohydride → HCID 24989422, compound

https://huagongshe.com/reaction/216632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 59189810HCID 59189810—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 24989422HCID 2498942258.7%

Reaction Steps

Sodium borohydride (0.23 g, 6.2 mmol) was added to a solution mixture of 2-aminocarbonylamino-6-(3-formylphenyl)indole-3-carboxamide (Compound 4-69, 1.0 g, 3.1 mmol) in anhydrous methanol and anhydrous tetrahydrofuran (methanol/tetrahydrofuran=1/1, 60 mL) under ice-cooling, and the mixture was stirred at room temperature overnight. After the reaction mixture was concentrated under reduced pressure, the precipitated solid was washed with water (30 mL), ethyl acetate (30 mL), and dried under reduced pressure to give the title compound (0.59 g) as a brown solid (yield 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193237B2
Source datasetuspto-grants-2012_06
ORD IDord-be7bd49b556446fc9c798d2da9ee99e6
Source noteuspto-grants-2012_06