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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623323Generated: October 31, 2026

Water → HCID 178512452, compound

https://huagongshe.com/reaction/623323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmantadineHCID 2130—
Reactant1,3-DI-Boc-2-methylisothioureaHCID 546603—
CatalystMercuric ChlorideHCID 24085—
SolventDimethylformamideHCID 6228—
ProductHCID 178512452HCID 178512452—

Reaction Steps

Amantadine (0.30 g, 2 mmol), HgCl2 (0.54 g, 2 mmol), and 1,3-bis(tert-butoxycarbonyl)-2-methyl-2-thiopseudourea (0.58 g, 2 mmol) were stirred in DMF (10 mL) under a N2 atmosphere for 24 h. H2O was added to the reaction mixture, and the white precipitate was removed by filtration. The precipitate was washed with CH2Cl2 twice, and the combined filtrate was extracted with CH2Cl2, washed with brine and dried over MgSO4, concentrated in vacuo, and purified by flash chromatography. The Boc protecting group was removed by 50% TFA/CH2Cl2 for 2 h at RT. Excess TFA was removed by passing N2 through the solution to give a yellow solid which was subsequently purified by flash chromatography (0.41 g, 74% over two steps). 1H-NMR (360 MHz, CD3OD) δ 2.13 (br s, 3H), 1.97 (br s, 6H), 1.76 (br s, 6H); 13C-NMR (90 MHz, CD3OD) δ 160.35, 53.83, 42.45, 36.86, 31.03; ESI-MS: Calculated for C11H19N3 (M+H)+ 194.2. Found: 194.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09301950B2
Source datasetuspto-grants-2016_04
ORD IDord-8557071a1acd40979849fb811e0399ee
Source noteuspto-grants-2016_04