Hydrochloric Acid → HCID 131719475, compound

HRID 974957Notes

Reaction equation

HRID 974957 reaction equation
O.[ClH:2].Cl.[O:4]1[C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=2[CH2:7][CH2:6][C@@H:5]1[CH2:14][NH:15][CH2:16][CH2:17][CH2:18][NH:19][C:20]1[N:25]=[CH:24][CH:23]=[CH:22][N:21]=1.[O:26]1[C:31]2[CH:32]=[CH:33][CH:34]=[CH:35][C:30]=2[CH2:29][CH2:28][C@@H:27]1[CH2:36][NH:37][CH2:38][CH2:39][CH2:40][NH:41][C:42]1[N:47]=[CH:46][CH:45]=[CH:44][N:43]=1.Cl.Cl.Cl.[H][H]>CO.CC(O)C.[Pd]>[OH2:4].[ClH:2].[ClH:2].[O:26]1[C:31]2[CH:32]=[CH:33][CH:34]=[CH:35][C:30]=2[CH2:29][CH2:28][C@@H:27]1[CH2:36][NH:37][CH2:38][CH2:39][CH2:40][NH:41][C:42]1[NH:47][CH2:46][CH2:45][CH2:44][N:43]=1.[O:4]1[C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=2[CH2:7][CH2:6][C@@H:5]1[CH2:14][NH:15][CH2:16][CH2:17][CH2:18][NH:19][C:20]1[NH:25][CH2:24][CH2:23][CH2:22][N:21]=1.[ClH:2].[ClH:2]

Participants

7

Procedure

A mixture of 3.6 g of (-)-(R)-N-[(3,4-dihydro-2H-1-benzopyran-2-yl)methyl]-N'-(2-pyrimidinyl)-1,3-propanediamine dihydrochloride hemihydrate in 150 ml of methanol and 20 ml of 2-propanol saturated with HCl was hydrogenated in the presence of 1.5 g of palladium-on-charcoal catalyst (2%). After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The product was crystallized from acetonitrile, filtered off and dried, yielding 2.7 g (74.0%) of (-)-(R)-N-[(3,4-dihydro-2H-1-benzopyran-2-yl) methyl]-N'-(1,4,5,6-tetrahydro-2-pyrimidinyl)-1,3-propanediamine dihydrochloride hemihydrate; mp. 200.2° C. [α]D20 =-60.97° (conc.=1% in CH3OH) (comp. 62).

Workup

  1. filtrationthe catalyst was filtered off
  2. customthe filtrate was evaporated
  3. customThe product was crystallized from acetonitrile
  4. filtrationfiltered off
  5. customdried

Sources & evidence

ORD record
ord-e9762981973648f88f12d7d5179c292b
Source dataset
uspto-grants-1997_03
Patent number
US05607949

Reaction notes

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