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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575160Generated: October 30, 2026

{[1-(methoxymethyl)cyclopropyl]methyl}amine hydrochloride → HCID 71715224, compound

https://huagongshe.com/reaction/575160

Reaction equation

Participants

RoleNameHCIDCharge
Reactant{[1-(methoxymethyl)cyclopropyl]methyl}amine hydrochlorideHCID 53398976—
Reactant2-Carbamoyl-9-fluoro-10-(3-hydroxy-3-methyl-but-1-ynyl)-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-3-carboxylic acidHCID 86693171—
ProductHCID 71715224HCID 71715224—

Reaction Steps

2-Carbamoyl-9-fluoro-10-(3-hydroxy-3-methyl-but-1-ynyl)-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-3-carboxylic acid (0.05 g) was reacted with 1-[1-(methoxymethyl)cyclopropyl]methanamine monohydrochloride similar to as described in Example 2 to afford 11 mg of 9-fluoro-10-(3-hydroxy-3-methyl-but-1-ynyl)-N3-[[1-(methoxymethyl)cyclopropyl]methyl]-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2,3-dicarboxamide following reverse phase hplc purification. MS (Q1) 471 (M)+. 1H NMR (400 MHz, DMSO) δ 11.34 (t, J=5.3 Hz, 1H), 8.60 (d, J=8.4 Hz, 1H), 8.38 (s, 1H), 7.90 (s, 1H), 7.01 (d, J=10.6 Hz, 1H), 5.48 (s, 1H), 5.09-4.88 (m, 2H), 4.67-4.44 (m, 2H), 3.25 (s, 4H), 1.49 (s, 5H), 0.63-0.30 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034866B2
Source datasetuspto-grants-2015_05
ORD IDord-3738b8d586d44a70b1304cba1e1c7cf3
Source noteuspto-grants-2015_05