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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575473Generated: October 30, 2026

(R)-2-(5-methylisoxazol-3-yl)but-3-yn-2-ol → (R)-3-cyclopropyl-9-fluoro-10-(3-hydroxy-3-(5-methylisoxazol-3-yl)but-1-yn-1-yl)-6,7-dihydro-5H-5,7-methanobenzo[c]imidazo[1,2-a]azepine-2-carboxamide

https://huagongshe.com/reaction/575473

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-2-(5-methylisoxazol-3-yl)but-3-yn-2-olHCID 58221468—
Reactant10-bromo-3-cyclopropyl-9-fluoro-6,7-dihydro-5H-5,7-methanobenzo[c]imidazo[1,2-a]azepine-2-carboxamideHCID 86693537—
Product(R)-3-cyclopropyl-9-fluoro-10-(3-hydroxy-3-(5-methylisoxazol-3-yl)but-1-yn-1-yl)-6,7-dihydro-5H-5,7-methanobenzo[c]imidazo[1,2-a]azepine-2-carboxamideHCID 86693540—

Reaction Steps

Similar to as described in General Procedure E, 10-bromo-3-cyclopropyl-9-fluoro-6,7-dihydro-5H-5,7-methanobenzo[c]imidazo[1,2-a]azepine-2-carboxamide was reacted with (R)-2-(5-methylisoxazol-3-yl)but-3-yn-2-ol to give the titled compound. MS+447.2. 1H NMR (400 MHz, DMSO) δ 8.68 (d, J=7.5 Hz, 1H), 7.45 (br s, 1H), 7.26 (d, J=10.1 Hz, 1H), 6.92 (br s, 1H), 6.57 (s, 1H), 6.35 (s, 1H), 5.26 (m, 1H), 3.68 (m, 1H), 314 (m, 1H), 2.41 (s, 3H), 1.82 (s, 3H), 1.77-1.61 (overlapping m, 3H), 0.99 (m, 1H), 0.68 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034866B2
Source datasetuspto-grants-2015_05
ORD IDord-b2ca8af19be64b0ba451826a21771ce8
Source noteuspto-grants-2015_05