Acetic Anhydride → HCID 70400636, compound

HRID 1981944Notes

Reaction equation

HRID 1981944 reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:8]2[C@@H:14]([OH:15])[C:13](=[O:16])[N:12]([CH2:17][CH2:18][N:19]([C:21]([O:23][CH2:24][C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)=[O:22])[CH3:20])[C:11]3[CH:31]=[CH:32][C:33]([CH3:35])=[CH:34][C:10]=3[S:9]2)=[CH:4][CH:3]=1.[C:36](OC(=O)C)(=[O:38])[CH3:37]>N1C=CC=CC=1>[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:8]2[C@@H:14]([O:15][C:36](=[O:38])[CH3:37])[C:13](=[O:16])[N:12]([CH2:17][CH2:18][N:19]([C:21]([O:23][CH2:24][C:25]3[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=3)=[O:22])[CH3:20])[C:11]3[CH:31]=[CH:32][C:33]([CH3:35])=[CH:34][C:10]=3[S:9]2)=[CH:4][CH:3]=1

Participants

4

Reactant 2

HCID 7918Acetic AnhydrideHCID 10791242HCID 10791242, compound

Product 1

HCID 70400636HCID 70400636, compound

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Procedure

A mixture of 0.73 g of (-)-cis-2-(4-methylphenyl)-3-hydroxy-5-[2-(N-benzyloxycarbonyl-N-methylamino)ethyl]-8-methyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one, 5 ml of acetic anhydride and 0.1 ml of pyridine is treated in the same manner as described in Example 1-(2), whereby 0.92 g of (-)-cis-2-(4-methylphenyl)-3-acetoxy-5-[2-(N-benzyloxycarbonyl-N-methylamino)ethyl]-8-methyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one is obtained as an oil. (3) A mixture of 0.92 g of (-)-cis-2-(4-methylphenyl)-3-acetoxy-5-[2-(N-benzyloxycarbonyl-N-methylamino)ethyl]-8-methyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one, 2 ml of 25% hydrogen bromide-acetic acid and 2 ml of acetic acid is stirred at room temperature for 2 hours. The mixture is evaporated under reduced pressure to remove solvent. Toluene is added to the residue, and the mixture is evaporated under reduced pressure to remove solvent. Ether is added to the residue, and the resultant crystals are collected by filtration and washed with ether. A mixture of the crystals thus obtained, 2 ml of ethanol and 2 ml of an aqueous 5% sodium hydroxide solution is stirred at room temperature for 2 hours. The mixture is adjusted to pH 8 with acetic acid, and then extracted with chloroform. The extract is washed with water, dried and evaporated under reduced pressure to remove solvent. The residue is converted to its hydrochloride and recrystallized from isopropanol. 0.32 g of (-)-cis-2-(4-methylphenyl)-3-hydroxy-5-[2-(N-methylamino)ethyl]-8-methyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one hydrochloride hemihydrate is obtained.

Workup

  1. additionis treated in the same manner

Sources & evidence

ORD record
ord-532f027c4a464f6592a2ba5c8abc3d60
Source dataset
uspto-grants-1986_06
Patent number
US04594342

Reaction notes

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