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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691477Generated: November 3, 2026

Dimethylformamide → 2-Hydroxy-N-methyl-2-[6-{[4-(trifluoromethoxy)phenyl]sulfonyl}-2-(trifluoromethyl)-6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepin-8-yl]acetamide

https://huagongshe.com/reaction/1691477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantMethylamine hydrochlorideHCID 6364545—
ReactantHydroxy[6-{[4-(trifluoromethoxy)phenyl]sulfonyl}-2-(trifluoromethyl)-6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepin-8-yl]acetic acidHCID 59618708—
Product2-Hydroxy-N-methyl-2-[6-{[4-(trifluoromethoxy)phenyl]sulfonyl}-2-(trifluoromethyl)-6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepin-8-yl]acetamideHCID 59618729—

Reaction Steps

A mixture of hydroxy[6-{[4-(trifluoromethoxy)phenyl]sulfonyl}-2-(trifluoromethyl)-6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepin-8-yl]acetic acid (51 mg, 0.091 mmol, Example 513), BOP (60.1 mg, 0.136 mmol), MeNH2—HCl (12.2 mg, 0.181 mmol), and diisopropylethylamine (0.08 ml, 0.453 mmol) in DMF was stirred for 2.5 h at rt. LC-MS showed the reaction complete. The solution was concentrated and the residue was purified by mass-directed HPLC eluting with H2O/MeCN/TFA (90:10:0.1-10:90:0.1) to give the title compound; Mass Spectrum: m/e=576 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153626B2
Source datasetuspto-grants-2012_04
ORD IDord-b23621d9c7254bc5bdbf09f59a046736
Source noteuspto-grants-2012_04