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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117763Generated: October 30, 2026

Triethylamine → HCID 69309075, compound

https://huagongshe.com/reaction/2117763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 69310638HCID 69310638—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 69309075HCID 6930907553%

Reaction Steps

Triethylamine (0.74 ml, 5.05 mmol), followed by methane sulphonyl chloride (0.103 ml, 1.33 mmol) was added to a stirred solution of 4-[2-(3,3-dimethyl-2-hydroxybut-1-yl)-1-(propyl)imidazol-5-yl]-2-anilinopyrimidine (Method 101; 480 mg, 1.26 mmol) in DCM (40 ml) at ambient temperature and the mixture stirred for 24 hours. The volatiles were removed by evaporation and toluene (10 ml), and 1,8-diazabicyclo[5.4.0]undec-7-ene (0.38 ml, 2.54 mmol) was added to the residue. The mixture was heated at reflux for 5 hours, allowed to cool, washed with water and extracted with EtOAc. The extracts were combined, dried and the solvent removed by evaporation to give the title compound (240 mg, 53%). NMR: 0.64 (t, 3H), 1.15 (s, 9H), 1.53 (q, 2H), 4.64 (t, 2H), 6.38 (d, 1H), 6.80 (d, 1H), 6.99 (t, 1H), 7.10 (d, 1H), 7.28 (t, 2H), 7.62 (d, 3H), 7.75 (s, 1H), 8.38 (d, 1H), 9.38 (s, 1H); m/z 362.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442697B2
Source datasetuspto-grants-2008_10
ORD IDord-1c8437d4f60c4403bedbf5f122ef9d08
Source noteuspto-grants-2008_10