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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402755Generated: November 1, 2026

Diisopropylethylamine → Tert-butyl 4-({1-[(6-methylpyridin-3-yl)carbonyl]azetidin-3-yl]carbonyl)-1,4-diazepane-1-carboxylate

https://huagongshe.com/reaction/1402755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant6-Methylnicotinoyl chlorideHCID 21890458—
ReactantTert-butyl 4-(azetidin-3-ylcarbonyl)-1,4-diazepane-1-carboxylateHCID 66739652—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-({1-[(6-methylpyridin-3-yl)carbonyl]azetidin-3-yl]carbonyl)-1,4-diazepane-1-carboxylateHCID 6673962536.4%

Reaction Steps

To a stirred solution of tert-butyl 4-(azetidin-3-ylcarbonyl)-1,4-diazepane-1-carboxylate (1.02 g, 3.6 mmol) and DIPEA (1.41 g, 10.8 mmol) in DCM (20 mL) was added a solution of 6-methylpyridine-3-carbonyl chloride (420 mg, 4.32 mmol) in DCM (5 mL) at 0° C. After 3 hours the reaction was diluted with DCM (10 mL), washed with saturated aqueous NaHCO3 (10 mL), brine (5 mL), dried (MgSO4), filtered and concentrated at reduced pressure. Purification by silica FCC (eluting with 100:0:0 to 95:4.5:0.5 gradient of DCM/MeOH/NH3) gave the title compound (527 mg, 36%) as an orange-brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912176B2
Source datasetuspto-grants-2014_12
ORD IDord-0d8891ce1c9244c98d578357879f29ec
Source noteuspto-grants-2014_12