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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591897Generated: October 31, 2026

Acetic Acid → HCID 58997392, compound

https://huagongshe.com/reaction/1591897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantN-(3-Aminophenyl)-2-chloro-4-fluorobenzamideHCID 16775600—
Reactanttert-Butyl (2R)-2-methyl-4-oxopiperidine-1-carboxylateHCID 25110958—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58997392HCID 5899739223%

Reaction Steps

Dissolve N-(3-amino-phenyl)-2-chloro-4-fluoro-benzamide (Preparation 1,200 mg, 0.756 mmol) and (2R)-2-methyl-4-oxo-piperidine-1-carboxylic acid tert-butyl ester (161 mg, 0.756 mmol) in tetrahydrofuran (5 mL). Add acetic acid (52 μl, 0.907 mmol) and sodium triacetoxyborohydride (192 mg, 0.907 mmol) and stir at room temperature for 18 hr. Heat the reaction to 45° C. for 4 hr. Cool the reaction to room temperature and load onto an SCX column with methanol. Wash the column with methanol, flush with 2M ammonia in methanol, and concentrate in vacuo. Purify by column chromatography (20%–75% ethyl acetate/hexane) to yield 80 mg (23%) of the title compound: mass spectrum (ion spray): m/z=462.4 (M+1); 1H NMR: δ (CDCl3, ppm) 7.76 (m, 2H), 7.20 (m, 1H), 7.15 (m, 1H), 7.10 (m, 1H), 6.70 (d, J=7.6 Hz, 1H), 6.40 (d, J=8.4 Hz, 1H), 4.20 (m, 1H), 3.82 (m, 2H), 3.67 (bs, 1H), 3.20 (m, 1H), 2.00 (m, 2H), 1.65 (m, 2H), 1.47 (s, 9H), 1.27, (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291632B2
Source datasetuspto-grants-2007_11
ORD IDord-e76bda23c753452a85810bd22ec0f04c
Source noteuspto-grants-2007_11