chloral hydrate
Bluelighter
- Joined
- Aug 23, 2009
- Messages
- 139
As far as I know, it is that polar -OH that stops ephedrine from crossing readily, it is speculated that if it did cross it would be very similar in effects to its 'cousins'
To continue my point, look: 2-benzylpiperidine crosses (analogous to methamphetamine), but with an -OH it is ritalinic acid (analogous to ephedrine) and doesn't cross, but with a reverse acetate ester it is phacetoperane (analogous to methylamphenidate) which does cross.
As such I think that "methylamphenidate" will cross and should be quite active. Furthermore if I'm correct with that acetic anhydride stuff, it should be extremely easy to make.
To continue my point, look: 2-benzylpiperidine crosses (analogous to methamphetamine), but with an -OH it is ritalinic acid (analogous to ephedrine) and doesn't cross, but with a reverse acetate ester it is phacetoperane (analogous to methylamphenidate) which does cross.
As such I think that "methylamphenidate" will cross and should be quite active. Furthermore if I'm correct with that acetic anhydride stuff, it should be extremely easy to make.
