関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | Sulfosalicylic Acid | HCID 7322 | — |
| 反応物 | Triphenylphosphine | HCID 11776 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Toluenesulfonate | HCID 3424274 | — |
| 生成物 | 2-Sulfooxybenzoate | HCID 21874451 | — |
反応手順
In a preferred embodiment, a mixture containing an 11a-halo-6-deoxy-6-demethyl-6-methylenetetracycline. preferably the p-toluene sulfonate of 11a-chloro methacycline; bis(triphenylphosphine)(hydroxylamine hydrochloride) dichloro rhodium (II) or its O-alkyl derivative complex, preferably hydroxylamine hydrochloride complex; and a tertiary phosphine, preferably triphenylphosphine, in methanol is subjected to agitation in a stainless steel autoclave, and hydrogenated at about 50° to 90° C. under a pressure between about 3 and 12 kg/cm2, prior to the termination of the reaction. Sulfosalicylic acid is added and the reaction mixture is cooled to about 0° C. for 2-4 hours. The alpha-6-deoxy-5-oxytetracyline sulfosalicylate, preferably doxycyline sulfosalicylate (or toluene sulfonate) thus obtained is filtered and washed with methanol.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04987242 |
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| 出典データセット | uspto-grants-1991_01 |
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| ORD ID | ord-9f3ad719ca1d48e0ab72c73a89429169 |
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| 出典メモ | uspto-grants-1991_01 |
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