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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644195Generated: October 25, 2026

Diisopropylethylamine → HCID 178455419, compound

https://huagongshe.com/reaction/1644195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Bromo-2-(2-bromo-ethyl)-benzenesulfonyl chlorideHCID 58016189—
ReactantHCID 137328873HCID 137328873—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 178455419HCID 17845541953.4%

Reaction Steps

The mixture of 5-[3-Amino-2-(tert-butyl-dimethyl-silanyloxymethyl)-phenyl]-1-methyl-3-[5-(morpholine-4-carbonyl)-pyridin-2-ylamino]-1H-pyridin-2-one (0.2 g, 0.36 mmol), 4-bromo-2-(2-bromo-ethyl)-benzenesulfonyl chloride (0.4 g, 1.08 mmol) and DIPEA (1 mL) in dichloroethane (10 mL) was microwaved at 120° C. for 30 min, then added 4-bromo-2-(2-bromo-ethyl)-benzenesulfonyl chloride (0.4 g, 1.08 mmol) and DIPEA (1 mL) and microwaved at 120° C. for 30 min. After repeating this process three times, the mixture was concentrated to afford a dark residue. Purification by silica gel chromatography (methylene chloride/acetone) afforded 0.15 g of 5-[3-(6-Bromo-1,1-dioxo-3,4-dihydro-1H-1lambda*6*-benzo[e][1,2]thiazin-2-yl)-2-(tert-butyl-dimethyl-silanyloxymethyl)-phenyl]-3-[5-(morpholine-4-carbonyl)-pyridin-2-ylamino]-1H-pyridin-2-one as a pale solid MS (ESI) 796.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124604B2
Source datasetuspto-grants-2012_02
ORD IDord-55df895ee03440ffb460eba83479d9ef
Source noteuspto-grants-2012_02