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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 563863Generated: October 30, 2026

HCID 1476965, compound → HCID 57833087, compound

https://huagongshe.com/reaction/563863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 1476965HCID 1476965—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 86622701HCID 86622701—
SolventMethanolHCID 887—
ProductHCID 57833087HCID 5783308758.3%

Reaction Steps

3-[(Dimethylamino)methylene]-1-methylpiperidin-4-one (9.04 g, 53.7 mmol) and tert-butyl {(3R)-1-[amino(imino)methyl]pyrrolidin-3-yl}carbamate hydrochloride (14.2 g, 53.7 mmol) were dissolved in methanol (100 mL) and to this was added dropwise sodium methoxide (9.66 g of a 30% solution in methanol). The reaction mixture was refluxed for 3 hours and then cooled to room temperature. The reaction mixture was then evaporated to dryness, and the residue was treated with water (50 mL). The precipitate was separated by filtration, washed with water (25 mL) and diethyl ether (50 mL) and dried to give the title compound 10.43 g (yield 58%). LCMS (ES+) M+H 334. 1H NMR (DMSO-d6) 1.39 (s, 9H) 1.85 (m, 1H) 2.13 (m, 1H) 2.33 (s, 3H) 2.60 (m, 2H) 2.67 (m, 2H) 3.23-3.26 (m, 1H) 3.31-3.37 (m, 3H) 3.40-3.536 (m, 1H) 3.63 (m, 1H) 4.04 (br s, 1H) 7.20 (br s, 1H) 8.04 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067589B2
Source datasetuspto-grants-2011_11
ORD IDord-c790fcdae69d440d89e7ed6535005e89
Source noteuspto-grants-2011_11