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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638964Generated: October 31, 2026

HCID 86618873, compound → HCID 9975171, compound

https://huagongshe.com/reaction/638964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86618873HCID 86618873—
ReactantHCID 178418361HCID 178418361—
ProductHCID 9975171HCID 997517190%

Reaction Steps

(+)-trans-1-(3,4-Dimethoxy-5-propylbenzoyl)-3-ethylazetidine-2-carboxylic acid hydroxyamide was prepared from (+)-trans-1-(3,4-dimethoxy-5-propylbenzoyl)-3-ethylazetidine-2-carboxylic acid benzyloxyamide by following Method H in 90% yield. The reaction was conducted at room temperature using a balloon of hydrogen for 1 h. ESMS: 351.6 [M+H]. 1H NMR (300 MHz, CD3OD): 6.93 (s, 1H), 6.90 (s, 1H), 4.80 (m, 1H), 4.48 (m, 1H), 4.32 (m, 1H), 3.75 (s, 3H), 3.71 (s, 3H), 2.62 (m, 1H), 2.49 (t, 2H), 1.85 (m, 1H), 1.72 (m, 1H), 1.50 (m, 2H), 0.84 (t, 6H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691843B2
Source datasetuspto-grants-2010_04
ORD IDord-4b786275f4fc4aafb01b547c79bf74f2
Source noteuspto-grants-2010_04