Hydrochloric Acid → De(2,3-dihydroxy) Nadolol Hydrochloride

HRID 2198848Notes

Reaction equation

HRID 2198848 reaction equation
[ClH:1].[C:2]1([O:12][CH2:13][CH:14]([OH:21])[CH2:15][NH:16][C:17]([CH3:20])([CH3:19])[CH3:18])[C:11]2[CH2:10][CH2:9][CH2:8][CH2:7][C:6]=2[CH:5]=[CH:4][CH:3]=1>>[ClH:1].[C:2]1([O:12][CH2:13][CH:14]([OH:21])[CH2:15][NH:16][C:17]([CH3:19])([CH3:18])[CH3:20])[C:11]2[CH2:10][CH2:9][CH2:8][CH2:7][C:6]=2[CH:5]=[CH:4][CH:3]=1

Participants

3

Reactant 2

HCID 313Hydrochloric AcidHCID 12445684Nadolol EP Impurity G

Product 1

HCID 20517342De(2,3-dihydroxy) Nadolol HydrochlorideYield 70%

Procedure

1-(tert.-butyl)-3-azetidinol and 5,6,7,8-tetrahydro-α-naphthol were reacted in the same manner as in Example 1 to form 1-(5,6,7,8-tetrahydro-α-naphthoxy)-3-(tert.-butylamino)-2-propanol. A hydrochloric acid gas was blown into the obtained propanol. As a result, 1-(5,6,7,8-tetrahydro-1-naphthoxy)-3-(tert.-butylamino)-2-propanol hydrochloride having a melting point of 148°-150° C. was obtained. The yield was 70%.

Sources & evidence

ORD record
ord-544bba62bd3b47df803b65cfe594cb2f
Source dataset
uspto-grants-1982_11
Patent number
US04360464

Reaction notes

Loading…