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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839602Generated: November 3, 2026

Methane → HCID 68125504, compound

https://huagongshe.com/reaction/839602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantHydrochloric AcidHCID 313—
ReactantDopamine HydrochlorideHCID 65340—
ReactantN-(2,2-Diethoxyethyl)-1-methyl-1H-tetrazol-5-amineHCID 13139802—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 68125504HCID 68125504—

Reaction Conditions

Temperature60 °C

Reaction Steps

(1-methyl-1H-tetrazol-5-yl)aminoacetaldehyde diethyl acetal (21.5 g.) and 3,4-dihydroxyphenethylamine hydrochloride (14.6 g.) were added to a mixture of ethanol (130 ml.) and water (35 ml.), and dissolved with heating and stirring. Conc. hydrochloric acid (10.5 ml.) was added thereto and the mixture was refluxed for 8 hours. The reaction mixture was treated with activated charcoal. The charcoal was filtered and washed with ethanol, after which the filtrate and the washings were combined and concentrated under reduced pressure. The residual crystals were recrystallized from a mixture of water and isopropyl alcohol and the obtained crystals (22.5 g.) were warmed for 16 hours at 60° C under reduced pressure to remove excess hydrogen chloride. The crystals were recrystallized from a mixture of a small amount of water, methanol and ether to give 1-(1-methyl-1H-tetrazol-5-yl)aminomethyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride trihemihydrate (15 g.), mp 107° to 110° C. Infrared Absorption Spectrum (Nujol) 1604, 1460 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04096263
Source datasetuspto-grants-1978_06
ORD IDord-dfc30cbb62c842dfa8f0fddcbe147968
Source noteuspto-grants-1978_06