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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591857Generated: November 1, 2026

Acetic Acid → HCID 58997377, compound

https://huagongshe.com/reaction/1591857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1-Methyl-4-piperidoneHCID 74049—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-butyl N-(3-aminophenyl)carbamateHCID 12877220—
SolventDichloromethaneHCID 6344—
ProductHCID 58997377HCID 58997377—

Reaction Steps

Combine (3-aminophenyl)carbamic acid tert-butyl ester (0.156 g, 0.756 mmol), 1-methylpiperidin-4-one (0.093 mL, 0.756 mmol), sodium triacetoxyborohydride (208 mg, 0.982 mmol), acetic acid (0.043 mL, 0.756 mmol) and dichloromethane (8 mL). Stir at room temperature overnight. Dilute with dichloromethane (5 mL) and wash twice with sodium hydroxide (10 mL 1N aq.). Combine the organic layers and wash with saturated aqueous NaCl (10 mL). Dry over magnesium sulfate, filter under reduced pressure and concentrate to dryness. Purify by flash chromatography on a Biotage® silica cartridge eluting with a 20/1 mixture of dichloromethane and 2N ammonia in methanol to give the free base of the title compound. Dissolve the residue in diethyl ether and treat with ethereal hydrogen chloride. Triturate the resulting gum with ether to give the title compound as a white solid: mp 124–5° C.; mass spectrum (ion spray): m/z =306.2 (M+1), 1H NMR (CDCl3): 7.06 (t, J=8.0 Hz, 1H), 6.86 (bs, 1H), 6.51–6.48 (m, 1H), 6.42 (bs, 1H), 6.30–6.27 (m, 1H), 3.60 (bs, 1H), 3.30 (bs, 1H), 2.80 (bd, J=11.8 Hz, 2H), 2.31 (s, 3H), 2.19–2.02 (m, 4H), 1.89 (bs, 2H), 1.52 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291632B2
Source datasetuspto-grants-2007_11
ORD IDord-1c69f38e3a6340c196afe3cfc907674b
Source noteuspto-grants-2007_11