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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987374Generated: November 1, 2026

Diisopropylethylamine → HCID 67422203, compound

https://huagongshe.com/reaction/1987374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 5-bromovalerateHCID 84580—
Reactant3,3''-Dimethyl-1',2',3',4',5', 6'-hexahydro-cis-[2,2';6',2'']terpyridineHCID 57591137—
SolventAcetonitrileHCID 6342—
ProductHCID 67422203HCID 6742220394.1%

Reaction Steps

A solution of (2′R,6′S)-3,3″-dimethyl-1′,2′,3′,4′,5′,6′-hexahydro-[2,2′;6′,2″]terpyridine (306 mg, 1.12 mmol), 5-bromo-pentanoic acid ethyl ester (263 mg, 1.12 mmol), DIPEA (260 μL, 1.49 mmol) and KI (10 mg, 0.060 mmol) in CH3CN (12 mL) was warmed to 60° C. and stirred for 23 h according to General Procedure A. Purification by flash chromatography on silica gel using CH2Cl2/MeOH/NH4OH (94:5:1) afforded 5-((2′R,6′S)-3,3″-dimethyl-3′,4′,5′,6′-tetrahydro-2′H-[2,2′;6′,2″]terpyridin-1′-yl)-pentanoic acid ethyl ester (417 mg, 90%) as a yellow oil. 1H NMR (CDCl3) δ 0.75-0.94 (m, 3H), 1.17 (t, 3H, J=7.1 Hz), 1.55-2.01 (m 8H), 2.20-2.35 (m, 6H), 2.47 (s, 6H), 3.99 (q, 2H, J=7.2 Hz), 7.05-7.09 (m, 2H), 7.43 (d, 2H, J=7.6 Hz), 8.46 (bs, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550484B2
Source datasetuspto-grants-2009_06
ORD IDord-682e88f32c584847a83b5b8a85883d60
Source noteuspto-grants-2009_06