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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575398Generated: October 29, 2026

Diisopropylamine → HCID 178495553, compound

https://huagongshe.com/reaction/575398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant1-Methoxy-2-methylbut-3-yn-2-olHCID 21706426—
ReactantHCID 178513780HCID 178513780—
SolventDimethylformamideHCID 6228—
ProductHCID 178495553HCID 17849555326.3%

Reaction Steps

3-(3-cyclopropyl-1H-1,2,4-triazol-5-yl)-9-fluoro-10-(3-hydroxy-4-methoxy-3-methyl-but-1-ynyl)-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2-carboxamide was prepared similarly according to General Procedure E with slight modification. 10-bromo-3-(3-cyclopropyl-1H-1,2,4-triazol-5-yl)-9-fluoro-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2-carboxamide was reacted with 1-methoxy-2-methyl-but-3-yn-2-ol in a solution of DMF (1.3 mL/mmol) and diisopropylamine (2.6 mL/mmol) to afford 17 mg of the titled compound (26.3% yield). M+1=467.2. 1H NMR (400 MHz, DMSO-d6) δ 8.65 (d, J=8.3 Hz, 1H), 8.38 (br s, 1H), 7.79 (br s, 1H), 7.05 (d, J=10.4 Hz, 1H), 5.66 (s, 1H), 5.00-4.81 (m, 2H), 4.65-4.52 (m, 2H), 3.47-3.34 (m, 2H), 3.37 (s, 3H), 2.13-2.04 (m, 1H), 1.45 (s, 3H), 1.03-0.95 (m, 2H), 0.93-0.87 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034866B2
Source datasetuspto-grants-2015_05
ORD IDord-37d9a5dbdc3f41f1bfa0a95302a3d557
Source noteuspto-grants-2015_05