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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1408984생성일: 2026년 10월 26일

Sodium Hydroxide → 4-(((1R,3S)-3-((tert-butoxycarbonyl)amino)-2,2,3-trimethylcyclopentyl)amino)-3-carbamoylpyrrolo[1,2-b]pyridazine-6-carboxylic acid

https://huagongshe.com/reaction/1408984

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물ethyl 4-((1R,3S)-3-(tert-butoxycarbonylamino)-2,2,3-trimethylcyclopentylamino)-3-carbamoylpyrrolo[1,2-b]pyridazine-6-carboxylateHCID 86707717—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물4-(((1R,3S)-3-((tert-butoxycarbonyl)amino)-2,2,3-trimethylcyclopentyl)amino)-3-carbamoylpyrrolo[1,2-b]pyridazine-6-carboxylic acidHCID 86707716112.1%

반응 조건

온도70 °C

반응 단계

A solution of ethyl 4-((1R,3S)-3-(tert-butoxycarbonylamino)-2,2,3-trimethylcyclopentylamino)-3-carbamoylpyrrolo[1,2-b]pyridazine-6-carboxylate (10.62 g, 22.42 mmol) and 1 N NaOH (120 mL) in THF (100 mL) and MeOH (100 mL) was heated to 60° C. for 16 hrs. and then the reaction mixture was added 120 ml of 1 N NaOH solution and heated to 70° C. for 8 hrs. The reaction mixture was added 120 ml of 1 N NaOH solution and heated to 70° C. for 8 hrs which was concentrated to remove THF and MeOH. The aqueous layer was acidified with conc. HCl solution until pH about 4 at 0-5° C. The solid was collected to give 4-(((1R,3S)-3-((tert-butoxycarbonyl)amino)-2,2,3-trimethylcyclopentyl)amino)-3-carbamoylpyrrolo[1,2-b]pyridazine-6-carboxylic acid (11.2 g, 76% yield). HPLC retention time=3.020 min., LC/MS (M+H)+=446.3.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08921368B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-84bca8cbd5ac4b1d814801fa8a27a16e
출처 메모uspto-grants-2014_12