HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405946Generated: October 31, 2026
Sodium Bicarbonate → HCID 68155180, compound
https://huagongshe.com/reaction/1405946
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (5-(4-(4-((3-Fluorobenzyl)oxy)-3-chloroanilino)-6-quinazolinyl)-2-furancarboxaldehyde | HCID 11181296 | — |
| Reactant | N-(2-aminoethyl)methanesulfonamide hydrochloride | HCID 22609809 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | HCID 68155180 | HCID 68155180 | 45% |
Reaction Steps
At room temperature, 10.0 g of compound 5-(4-(4-(3-fluorobenzyloxy)-3-chloroanilino)-6-quinazolinyl)furan-2-formaldehyde, 6.5 g of compound N-(2-aminoethyl)methanesulfonamide hydrochloride, and 14.6 g of triethylamine in the mixture of dichloromethane/methanol (3:1) were stirred overnight, then cooled with ice-bath to 0° C., and 1.4 g of sodium borohydride was added at that temperature. The mixture was warmed to room temperature, stirred overnight, saturated sodium bicarbonate was added to quench the reaction, and extracted with ethyl acetate. The organic phase was washed with saturated sodium chloride solution, dried over anhydrous sodium sulfate, and subjected to a column chromatography to obtain 5.7 g of the desired product, yield 45.0%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916574B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-a58cb3cc806146349e7a0c0423e309f7 |
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| Source note | uspto-grants-2014_12 |
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