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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697462Generated: October 31, 2026

Methanamine, N-methoxy-, hydrochloride (1:1) → HCID 58125481, compound

https://huagongshe.com/reaction/1697462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant6,7-Dihydro-5H-pyrazolo[5,1-b][1,3]oxazine-3-carboxylic acidHCID 52228125—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetonitrileHCID 6342—
ProductHCID 58125481HCID 5812548188.2%

Reaction Steps

To a stirred solution of 6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine-3-carboxylic acid (8.14 g, 48.4 mmol), N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (10.21 g, 53.3 mmol), 1-hydroxybenzotriazole hydrate (8.16 g, 53.3 mmol), 4-dimethylaminopyridine (300 mg, 2 mmol), and DIPEA (16.5 mL, 97 mmol) in anhydrous acetonitrile (200 mL) was added a solution of N,O-dimethylhydroxylamine hydrochloride (9.44 g, 97 mmol) and DIPEA (16.5 mL, 97 mmol) in anhydrous acetonitrile (100 mL). The mixture was stirred for 3 days at room temperature, then poured into saturated NaHCO3 solution (200 mL) and extracted with EtOAc (3×1000 mL). The combined organic layers were washed with brine (200 mL), dried (Na2SO4), filtered and concentrated. Flash chromatography (0 to 5% MeOH in DCM) afforded the amide as a solid (9.02 g, 88%). 1H NMR (400 MHz, DMSO-d6) δ7.62 (s, 1H), 4.35 (t, 2H, J=5.24 Hz), 4.08 (t, 2H, J=6.20 Hz), 3.63 (s, 3H), 3.12 (s, 3H), 2.20-2.15 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163901B2
Source datasetuspto-grants-2012_04
ORD IDord-ef4c4f76913e43a2aabb440b127fecf8
Source noteuspto-grants-2012_04