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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478137Generated: November 1, 2026

Sodium cyanoborohydride → HCID 90260014, compound

https://huagongshe.com/reaction/1478137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 67155917HCID 67155917—
ReactantHCID 90258783HCID 90258783—
SolventAcetic acid methanolHCID 10129899—
ProductHCID 90260014HCID 90260014—

Reaction Steps

1-(5-Amino-1H-pyrrolo[2,3-b]pyridin-2-yl)-ethanone (1 eq) and 3-Formyl-N-pyridin-3-yl-benzamide (1.1 eq) were stirred in a mixture of MeOH/AcOH (10/1; 0.06M) for 2 h. Then NaBH3CN (1.2 eq) was slowly added and the mixture was stirred under argon at RT overnight. The reaction was quenched by addition of saturated NaHCO3 solution until neutrality. MeOH and acetic acid were evaporated. The crude was filtered and washed with water and Et2O before being purified on reverse phase (H2O 1% TFA/MeCN 1% TFA 100/0, 0/100). MeCN was evaporated. The product was suspended in H2O and basified with saturated NaHCO3 solution until pH=8-9. The aqueous layer was extracted three times with AcOEt. The organic layer was dried over Na2SO4, filtered and concentrated to give the expected product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403823B2
Source datasetuspto-grants-2016_08
ORD IDord-ff39d62637dd4ec1a04e8ae9c6d6b11b
Source noteuspto-grants-2016_08