Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630351Generated: November 2, 2026

1-methyl-5-(tributylstannyl)-1H-1,2,3-triazole → HCID 71577060, compound

https://huagongshe.com/reaction/1630351

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-methyl-5-(tributylstannyl)-1H-1,2,3-triazoleHCID 22609826—
ReactantHCID 86688212HCID 86688212—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 71577060HCID 7157706044.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of N2-(4-bromo-2-chloro-5-methoxyphenyl)-N4-methyl-5-(trifluoromethyl)pyrimidine-2,4-diamine (50 mg, 0.12 mmol), 1-methyl-5-(tributylstannyl)-1H-1,2,3-triazole (68 mg, 0.18 mmol) and Pd(dppf)2Cl2 (10 mg, 0.012 mmol) in dioxane (4 mL) was degassed under a stream of nitrogen for 10 min. The reaction mixture was heated to 100° C. for 18 h. Further amounts of 1-methyl-5-(tributylstannyl)-1H-1,2,3-triazole (68 mg, 0.18 mmol) and Pd(dppf)2Cl2 (10 mg, 0.012 mmol) were added and the mixture maintained at 100° C. for another 24 h, after which further amounts of 1-methyl-5-(tributylstannyl)-1H-1,2,3-triazole (68 mg, 0.18 mmol) and Pd(dppf)2Cl2 (10 mg, 0.012 mmol) were added. The mixture was maintained at 100° C. for another 48 h. The mixture was cooled and concentrated to dryness under vacuum, and the residue partitioned between DCM and water. The separated organic phase was concentrated to dryness under vacuum and the residue purified by RP-HPLC; the product was isolated as a cream solid (22 mg, 44%). LCMS (ESCI_Formic_MeCN): [MH+]=414 at 3.45 min. 1H NMR δ (DMSO-d6): 8.58 (s, 1H); 8.16 (s, 1H); 7.98 (s, 1H); 7.71 (s, 1H); 7.42 (s, 1H); 7.24 (d, J=5.1, 1H); 3.82 (s, 3H); 3.76 (s, 3H); 2.87 (d, J=4.4, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791130B2
Source datasetuspto-grants-2014_07
ORD IDord-c74a671295264552a270e1911d55cefd
Source noteuspto-grants-2014_07