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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1922191생성일: 2026년 10월 26일

tert-Butyl carbazate → 4-(2-(Cyclohexylmethylamino)benzo[d]oxazol-6-yloxy)pyridine-2-carbohydrazide

https://huagongshe.com/reaction/1922191

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl carbazateHCID 70091—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물4-(2-(Cyclohexylmethylamino)benzo[d]oxazol-6-yloxy)pyridine-2-carboxylic acidHCID 57725514—
용매TriethylamineHCID 8471—
생성물4-(2-(Cyclohexylmethylamino)benzo[d]oxazol-6-yloxy)pyridine-2-carbohydrazideHCID 57725456—

반응 단계

In Scheme 5, 4-(2-(methylsulfinyl)benzo[d]oxazol-6-yloxy)-N-methylpyridine-2-carboxamide is aminated with cyclohexylmethanamine. The resulting 4-(2-(cyclohexylmethylamino)benzo[d]oxazol-6-yloxy)-N-methylpyridine-2-carboxamide is then hydrolyzed to form 4-[2-(cyclohexylmethyl-amino)-benzooxazol-6-yloxy]-pyridine-2-carboxylic acid. 4-[2-(Cyclohexylmethyl-amino)-benzooxazol-6-yloxy]-pyridine-2-carboxylic acid then reacts with benzotriazol-1-yloxytris(dimethylamino)-phosphonium hexafluorophosphate, tert-butyl carbazate, and triethyl amine to form 4-(2-(cyclohexylmethylamino)benzo[d]oxazol-6-yloxy)pyridine-2-carbohydrazide. 4-(2-(Cyclohexylmethylamino)benzo[d]oxazol-6-yloxy)pyridine-2-carbohydrazide then reacts with trimethyl orthoformate to form a compound of the embodiments.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08173689B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-e6d31287251b47a9a5eb4770b9cb04db
출처 메모uspto-grants-2012_05