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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499402Generated: October 30, 2026

Diisopropylethylamine → HCID 86726656, compound

https://huagongshe.com/reaction/1499402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-butyl N-[(3S)-piperidin-3-yl]carbamateHCID 1514171—
ReactantHCID 14207943HCID 14207943—
Solvent1-ButanolHCID 263—
ProductHCID 86726656HCID 8672665694%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a vial containing 4-chloro-5-nitrothieno[2,3-b]pyridine (138.2 mg, 0.6439 mmol) and tert-butyl (3S)-piperidin-3-ylcarbamate (Combi-Blocks, 325.5 mg, 1.625 mmol), 1-butanol (3.00 mL) was added, followed by DIPEA (201.4 mg, 1.558 mmol), then the mixture was stirred at 110° C. for 12 h. After cooling to room temperature, the reaction mixture was concentrated under reduced pressure. The resulting residue was purified by chromatography on silica gel (0-100% EtOAc in hexanes) to give the title compound as a yellow solid (228.4 mg, 94%). LCMS calc. for C17H23N4O4S (M+H)+: m/z=379.1. found 379.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09200004B2
Source datasetuspto-grants-2015_12
ORD IDord-63c92fd019334592987c76a2c57a872f
Source noteuspto-grants-2015_12