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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575152Generated: October 26, 2026

2-Amino-2-methylpropionitrile → 9-Fluoro-3-(hydroxymethyl)-10-(3-hydroxy-3-methyl-but-1-ynyl)-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2-carboxamide

https://huagongshe.com/reaction/575152

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-2-methylpropionitrileHCID 88022—
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—
Product9-Fluoro-3-(hydroxymethyl)-10-(3-hydroxy-3-methyl-but-1-ynyl)-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2-carboxamideHCID 8669317224%

Reaction Steps

2-Carbamoyl-9-fluoro-10-(3-hydroxy-3-methyl-but-1-yn yl)-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-3-carboxylic acid (0.09 g) was reacted with 2-amino-2-methylpropionitrile similar to as described in Example 2 to afford 20.8 mg of 9-fluoro-3-(hydroxymethyl)-10-(3-hydroxy-3-methyl-but-1-ynyl)-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2-carboxamide following reverse phase hplc purification. MS (Q1) 440 (M)+. 1H NMR (400 MHz, DMSO) δ 12.25 (s, 1H), 8.65 (d, J=8.4 Hz, 1H), 8.58 (s, 1H), 8.07 (s, 1H), 7.03 (d, J=10.5 Hz, 1H), 5.50 (s, 1H), 5.10-4.93 (m, 2H), 4.64-4.46 (m, 2H), 1.70 (s, 6H), 1.49 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034866B2
Source datasetuspto-grants-2015_05
ORD IDord-c85e4f5956674f0882ad8c7e6f9b4bd5
Source noteuspto-grants-2015_05