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Tizanidine dosage 8mg /10mg. In the next step, we prepare 2-alkyl substituted alkyl analog of 3-nitropropylethyl nitrate using the procedure described in Example 1. The 2-alkyl substituted alkyl analog of 3-nitropropolethyl nitrate is prepared by substituting the amino group on C-1 position with a nitro group, such as an alkyl substituent. The 3-nitropropyl substituted alkyl analogue of 3-nitropropylethyl nitrate is prepared by substituting the nitrogen atom at 3 position of the phenyl ring with an alkyl group such as alkenyl or a cycloalkyl group. The alkyl group can be replaced by a C 3 -alkyl, 6 or 8 -alkyl group. Furthermore, a C 1 -alkyl substituent can be substituted at the 3 position of phenyl ring to yield a cyclic amide C 3 -alkyl. The 3-nitropropyl substituted alkyl Generic for adipex p phentermine 37.5 mg analogue of 3-nitropropolethyl nitrate is prepared by substituting the oxygen atom at 3 position with an alkyl group such as alkenyl or a cycloalkyl group. The alkyl group can be replaced by a C 1 -alkyl group, 3 a C 6 -alkyl group, or a C 8 -alkyl group. The cycloalkyl group can be replaced by a C 2 -alkyl group and the alkyl can be substituted for a cyclopropyl group. Example 9 The 1,3-propyl-1,3-nitro-3-nitropropyl nitrate is prepared by adding to a solution of the acetic anhydride in water, 1,3-propan-1-one, or 3-nitropropane (Example 4) the corresponding 3-nitropropyl-1,3-nitro-3-nitro-3-nitropropyl nitrate. acetic anhydride is prepared by mixing a 1,3-propan-1-one with ethyl acetate in water; 3-nitropropane is prepared by mixing propanoic acid with water and nitric acid. The 3,5-nitro-3,5-nitro-3-nitropropyl nitrate is prepared by adding to a solution of 3-nitro-3,5-nitro-3-nitropropyl nitrate in water, 1,3-propan-1-one, or 3-nitropropane (Example 4) the corresponding 3-nitropropyl-3,5-nitro-3-nitro-3-nitropropyl nitrate. acetic anhydride is prepared by mixing a 1,3-propan-1-one with ethyl acetate in water; 3-nitropropane is prepared by mixing propanoic acid with water and nitric acid. The 1,3-propan-1-one and 3,5-nitro-3,5-nitro-3-nitro-3-nitropropyl nitrate are used in the following reactions: Step 1: The 3-nitropropyl-3,5-nitro-3-nitro-3-nitropropyl nitrate is prepared by reacting the acetic anhydride with 1,3-propan-1-one. This reaction is completed at the temperature of about 50° C. Step 2: The 3,5-nitro-3,5-nitro-3-nitro-3-nitropropyl nitrate is prepared by reacting the acetic anhydride with 3-nitropropane. This reaction is completed at the temperature of about 50° C. Step 3: The 3-nitropropyl-3,5-nitro-3-nitro-3-nitropropyl nitrate is prepared by reacting the acetic anhydride with 1,3-propan-1-one and the corresponding 3-nitropropyl-3,5-nitro-3-nitro-3-nitropropyl nitrate. This reaction is completed at the temperature of about 50° C. The acetic anhydride is reacted with the corresponding 3-nitropropylene.
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