HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478137Generated: November 1, 2026
Sodium cyanoborohydride → HCID 90260014, compound
https://huagongshe.com/reaction/1478137
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 67155917 | HCID 67155917 | — |
| Reactant | HCID 90258783 | HCID 90258783 | — |
| Solvent | Acetic acid methanol | HCID 10129899 | — |
| Product | HCID 90260014 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09403823B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-ff39d62637dd4ec1a04e8ae9c6d6b11b |
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| Source note | uspto-grants-2016_08 |
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