1,4-Dioxane hydrochloride → N-(2-{[3-(fluoromethyl)pyrrolidin-3-yl]amino}-2-oxoethyl)-3-(trifluoromethyl)benzamide HCl salt

HRID 1809951노트

반응식

HRID 1809951 반응식
[F:1][CH2:2][C:3]1([NH:15][C:16](=[O:31])[CH2:17][NH:18][C:19](=[O:30])[C:20]2[CH:25]=[CH:24][CH:23]=[C:22]([C:26]([F:29])([F:28])[F:27])[CH:21]=2)[CH2:7][CH2:6][N:5](C(OC(C)(C)C)=O)[CH2:4]1.O1CCOCC1.[ClH:38]>C1COCC1>[ClH:38].[F:1][CH2:2][C:3]1([NH:15][C:16](=[O:31])[CH2:17][NH:18][C:19](=[O:30])[C:20]2[CH:25]=[CH:24][CH:23]=[C:22]([C:26]([F:29])([F:27])[F:28])[CH:21]=2)[CH2:7][CH2:6][NH:5][CH2:4]1

참가 물질

4

반응물 2

HCID 204431481,4-Dioxane hydrochlorideHCID 59556186Tert-butyl 3-(fluoromethyl)-3-[({[3-(trifluoromethyl)benzoyl]amino}acetyl)amino]pyrrolidine-1-carboxylate

생성물 1

HCID 66792273N-(2-{[3-(fluoromethyl)pyrrolidin-3-yl]amino}-2-oxoethyl)-3-(trifluoromethyl)benzamide HCl salt

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 578 mg (1.29 mmol) of tert-butyl 3-(fluoromethyl)-3-[({[3-(trifluoromethyl)benzoyl]amino}acetyl)amino]pyrrolidine-1-carboxylate in 5 mL of THF was added 2 mL of 4 N HCl dioxane solution. The reaction mixture was stirred at room temperature for 1 h and evaporated to give the yellow solid, N-(2-{[3-(fluoromethyl)pyrrolidin-3-yl]amino}-2-oxoethyl)-3-(trifluoromethyl)benzamide HCl salt: MS (m/e): 347 (M+1)+.

후처리

  1. customevaporated

출처 및 근거

ORD 기록
ord-f8594cda39aa485cb92aa434b8211e9e
출처 데이터셋
uspto-grants-2013_01
특허 번호
US08362003B2

반응 노트

불러오는 중…