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HRID 6213作成日:2026年10月23日

Hydrochloric Acid → HCID 178418664、化合物

https://huagongshe.com/ja/reaction/6213

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物3-AminopyridineHCID 10009—
反応物2-AminopyridineHCID 10439—
反応物Ammonium ChlorideHCID 25517—
反応物Di-tert-butyl dicarbonateHCID 90495—
反応物SulfurHCID 5362487—
反応物3-t-Butoxycarbonylamino-4-thia-pyridineHCID 67567623—
反応物ButyllithiumHCID 178418339—
溶媒Acetic AcidHCID 176—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 178418664HCID 178418664—

反応手順

In Scheme (3), 3-aminopyridine is acylated with di-t-butyldicarbonate to introduce the t-butoxycarbonyl (t-BOC) protecting group. (It will be appreciated that two other pyridinothiazolothio mercaptans may be prepared by known methodology using other amino pyridine isomers.) The t-BOC protected 3-aminopyridine is then treated with n-butyllithium in tetrahydrofuran followed by elemental sulfur (S8), followed by treatment with saturated ammonium chloride. The resulting 3-t-butoxycarbonylamino-4-thia-pyridine is treated with a mixture of acetic acid and HCl to provide 3-amino-4-mercaptopyridine hydrochloride. The desired 5-pyridinothiazolo thiomercaptan can then be prepared by treating this compound with carbon disulfide under basic conditions.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05247073
出典データセットuspto-grants-1993_09
ORD IDord-ed7c34e35eb445bc9fee78139710e092
出典メモuspto-grants-1993_09