Water → HCID 12773912, compound

HRID 1284064Notes

Reaction equation

HRID 1284064 reaction equation
[ClH:1].[OH:2][C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][C:11]=1[OH:12])[CH2:6][CH2:7][NH2:8].C(O[CH:16](OCC)[CH2:17][O:18][C:19]1[CH:23]=[N:22][S:21][N:20]=1)C.O>Cl.C(O)CCC>[ClH:1].[S:21]1[N:22]=[CH:23][C:19]([O:18][CH2:17][CH:16]2[C:9]3[C:5](=[CH:4][C:3]([OH:2])=[C:11]([OH:12])[CH:10]=3)[CH2:6][CH2:7][NH:8]2)=[N:20]1

Participants

6

Procedure

A mixture of 3,4-dihydroxyphenethylamine hydrochloride (1.62 g), (1,2,5-thiadiazol-3-yl)oxyacetaldehyde diethyl acetal (2.6 g), n-butanol (50 ml), water (25 ml) and 10% hydrochloric acid (3 drops) was refluxed for 15 hours. After the reaction, n-butanol was distilled off from the reaction mixture under reduced pressure. The residue was dissolved in water, and the solution was washed twice with chloroform and once with ether and then the aqueous layer was concentrated to give colourless crystals of 1-(1,2,5-thiadiazol-3-yl)oxymethyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride (2g). The product was recrystallized from aqueous methanol to give colourless crystals like cotton, mp 252°C (dec.).

Workup

  1. temperaturewas refluxed for 15 hours
  2. distillationwas distilled off from the reaction mixture under reduced pressure
  3. dissolutionThe residue was dissolved in water
  4. washthe solution was washed twice with chloroform and once with ether
  5. concentrationthe aqueous layer was concentrated

Sources & evidence

ORD record
ord-8b0e66c697ec48c59379bbf9e502ce90
Source dataset
uspto-grants-1976_08
Patent number
US03978063

Reaction notes

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