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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361389Generated: October 30, 2026

Acetic Acid → HCID 67994837, compound

https://huagongshe.com/reaction/2361389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-Formyl-5-methoxybenzoic acidHCID 7176205—
ReactantHCID 67994528HCID 67994528—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67994837HCID 67994837—

Reaction Steps

A mixture of 7-acetyl-1-(3-amino-2-methylphenyl)-5H-pyridazino[4,5-b]indole-4-carboxamide (0.250 g, crude product from the previous step), 2-formyl-5-methoxybenzoic acid (0.251 g, 1.391 mmol), sodium triacetoxyborohydride (0.442 g, 2.087 mmol), and acetic acid (0.100 mL, 1.739 mmol) in dichloromethane (18 mL) and tetrahydrofuran (18 mL) was stirred at room temperature for 3 hr. Additional sodium triacetoxyborohydride (0.442 g, 2.087 mmol) was added and the reaction mixture was stirred at rt. Three hours later, another portion of sodium triacetoxyborohydride (0.442 g, 2.087 mmol) was added, and the mixture was stirred at room temperature overnight. The reaction was quenched with water (30 mL) and the mixture was extracted with ethyl acetate (4×40 mL). The combined extract was dried over anhydrous MgSO4. Removal of solvent under vacuum provided the crude desired product (0.336 g) as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685969B2
Source datasetuspto-grants-2014_04
ORD IDord-a5196cdb585a4dcaac5c3f1a10411c5b
Source noteuspto-grants-2014_04