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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206333Generated: November 2, 2026

Sodium Bicarbonate → Tert-butyl 4-(5-formyl-6-hydroxypyridin-2-yl)-1,4-diazepane-1-carboxylate

https://huagongshe.com/reaction/2206333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantTert-butyl 1,4-diazepane-1-carboxylateHCID 2756058—
ReactantHCID 178519593HCID 178519593—
SolventDimethyl SulfoxideHCID 679—
ProductTert-butyl 4-(5-formyl-6-hydroxypyridin-2-yl)-1,4-diazepane-1-carboxylateHCID 178452079102.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

6-Chloro-2-hydroxynicotinaldehyde (1 g, 6.37 mmol) was dissolved in DMSO (12 mL) at room temperature. The solution was treated with tert-butyl 1,4-diazepane-1-carboxylate (2.55 g, 12.74 mmol) at room temperature. The reaction mixture was stirred at 100° C. for 2 hours and cooled to room temperature. An aqueous saturated NaHCO3 solution (50 mL) was added. The aqueous layer was extracted with CH2Cl2 three times. The combined organic layers were dried over K2CO3, filtered and concentrated under vacuum to give 2.1 g of tert-butyl 4-(5-formyl-6-hydroxypyridin-2-yl)-1,4-diazepane-1-carboxylate. The concentrated residue was used in next step without further purification. MS m/z 322 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371336B2
Source datasetuspto-grants-2016_06
ORD IDord-75cca1fd025e4c12bdfd3259d1840e85
Source noteuspto-grants-2016_06