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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275018Generated: October 31, 2026

Sodium Dithionite → tert-Butyl(1-(2-(1-ethyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-1-methyl-1H-benzo[d]imidazole-5-carbonyl)piperidin-3-yl)carbamate

https://huagongshe.com/reaction/2275018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium DithioniteHCID 24489—
Reactant1-Ethyl-1H-pyrrolo[2,3-b]pyridine-2-carbaldehydeHCID 86340174—
Reactanttert-Butyl(1(4-(methylamino)-3-nitrobenzoyl)piperidin-3-yl)carbamateHCID 118181215—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventSodium SulfateHCID 24436—
Producttert-Butyl(1-(2-(1-ethyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-1-methyl-1H-benzo[d]imidazole-5-carbonyl)piperidin-3-yl)carbamateHCID 11817862554%

Reaction Conditions

Temperature100 °C

Reaction Steps

Sodium hydrosulfite (235 mg, 1.150 mmol) dissolved in water (1.500 mL) was added to a solution of tert-butyl(1-(4-(methylamino)-3-nitrobenzoyl)piperidin-3-yl)carbamate (145 mg, 0.383 mmol) and 1-ethyl-1H-pyrrolo[2,3-b]pyridine-2-carbaldehyde (66.7 mg, 0.383 mmol) in ethanol (3 mL) at RT under nitrogen. The reaction mixture was heated to 100° C. in a microwave for 5 h. The reaction mixture was diluted with DCM (20 mL), Na2SO4 was added and the resultant suspension filtered and concentrated in vacuo to yield the crude product as a yellow oil. The crude product was purified by Biotage SP4 on a SNAP 25 g silica cartridge using a gradient of 0% (20% MeOH/DCM)/DCM→100% (20% MeOH/DCM)/DCM. Appropriate fractions were combined and evaporated under vacuum to give the title compound as a yellow solid (104 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09127003B2
Source datasetuspto-grants-2015_09
ORD IDord-7734909c2a2142b5b810cd45859a793c
Source noteuspto-grants-2015_09