Hydrochloric Acid → 6-[3-(1-Pyrrolidinyl)propylamino]-7,8,9,10-tetrahydro-1,2,4-triazolo[3,4-a]phthalazine dihydrochloride hemihydrate

HRID 1154021Notes

Reaction equation

HRID 1154021 reaction equation
[N:1]1([CH2:6][CH2:7][CH2:8][NH:9][C:10]2[C:19]3[CH2:18][CH2:17][CH2:16][CH2:15][C:14]=3[C:13]3=[N:20][N:21]=[CH:22][N:12]3[N:11]=2)[CH2:5][CH2:4][CH2:3][CH2:2]1.[ClH:23].C([OH:26])C>>[OH2:26].[ClH:23].[ClH:23].[N:1]1([CH2:6][CH2:7][CH2:8][NH:9][C:10]2[C:19]3[CH2:18][CH2:17][CH2:16][CH2:15][C:14]=3[C:13]3=[N:20][N:21]=[CH:22][N:12]3[N:11]=2)[CH2:2][CH2:3][CH2:4][CH2:5]1.[N:1]1([CH2:6][CH2:7][CH2:8][NH:9][C:10]2[C:19]3[CH2:18][CH2:17][CH2:16][CH2:15][C:14]=3[C:13]3=[N:20][N:21]=[CH:22][N:12]3[N:11]=2)[CH2:2][CH2:3][CH2:4][CH2:5]1.[ClH:23].[ClH:23]

Participants

4

Procedure

The amine obtained above was dissolved in ethanol and treated with an excess of ethereal hydrogen chloride. The solid which formed was separated by filtration to give 6-[3-(1-pyrrolidinyl)propylamino]-7,8,9,10-tetrahydro-1,2,4-triazolo[3,4-a]phthalazine dihydrochloride hemihydrate melting at about 277°-278° C.

Workup

  1. customThe solid which formed
  2. customwas separated by filtration

Sources & evidence

ORD record
ord-c1c1568c8cbf45c0b3738e0c5c8a424e
Source dataset
uspto-grants-1984_12
Patent number
US04487930

Reaction notes

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