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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131653생성일: 2026년 10월 25일

2-Tetralone → HCID 11705519, 화합물

https://huagongshe.com/reaction/131653

반응식

참여 물질

역할이름HCID투입량
반응물2-TetraloneHCID 68266—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물2-(S)-amino-pentanoic acid [5-(5-methoxy-1,5-dimethyl-hexyl)-thiazol-2-yl]-amide HCl saltHCID 131726918—
용매1,1-DichloroethaneHCID 6365—
생성물HCID 11705519HCID 11705519—
생성물HCID 11712247HCID 11712247—

반응 단계

A mixture of 2-(S)-amino-pentanoic acid [5-(5-methoxy-1,5-dimethyl-hexyl)-thiazol-2-yl]-amide HCl salt (600 mg, 1.59 mmol) and 2-tetralone (253 mg, 2.07 mmol) in dichloroethane was stirred at room temperature overnight. Sodium triacetoxyborohydride (530 mg, 2.5 mmol) was added and the mixture was stirred at room temperature overnight. The mixture was quenched with water, adjusted pH to around 10 and extracted with methylene chloride. The organic layer was concentrated to dryness. The residue was purified by SCX column after eluting with 1 M NH3/methanol and concentrated to dryness to give 620 mg that was purified by Shimadzu HPLC to give 2-(S)-(1,2,3,4-tetrahydro-naphthalen-2-ylamino)-pentanoic acid [5-(5-methoxy-1,5-dimethyl-hexyl)-thiazol-2-yl]-amide, LC-MS RT=2.2 min, M+1=472.5 as an oil and 2-(S)-(1,2,3,4-tetrahydro-naphthalen-2-ylamino)-pentanoic acid [5-(5-hydroxy-1,5-dimethyl-hexyl)-thiazol-2-yl]-amide, retention time, LC-MS RT=1.9 min, M+1=458.4 as a beige glass form.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384968B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-a1b977cb52b647f28a1188fb5c56bd23
출처 메모uspto-grants-2008_06