Hydrochloric Acid → Hydrochloric Acid

HRID 2284776노트

반응식

HRID 2284776 반응식
[Cl:1][C:2]1[N:7]=[C:6]([NH:8][CH2:9][CH2:10][CH3:11])[C:5]([C:12]#[C:13][CH2:14][CH2:15][CH2:16][NH:17][C:18](=[O:30])[C@@H:19]([N:21](C)[C:22](=O)OC(C)(C)C)[CH3:20])=[CH:4][N:3]=1.[ClH:31]>O1CCOCC1>[Cl:1][C:2]1[N:7]=[C:6]([NH:8][CH2:9][CH2:10][CH3:11])[C:5]([C:12]#[C:13][CH2:14][CH2:15][CH2:16][NH:17][C:18](=[O:30])[C@@H:19]([NH:21][CH3:22])[CH3:20])=[CH:4][N:3]=1.[ClH:31]

참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 90052304(S)-tert-butyl (1-((5-(2-chloro-4-(propylamino)pyrimidin-5-yl)-4-pentyn-1-yl)amino)-1-oxopropan-2-yl)(methyl)carbamate

생성물 2

HCID 313Hydrochloric AcidHCID 90052759(S)-N-(5-(2-chloro-4-(propylamino)pyrimidin-5-yl)-4-pentyn-1-yl)-2-(methylamino)propanamide

시약·촉매·용매 1

HCID 312751,4-Dioxane용매2회

실험 절차

To a solution of (S)-tert-butyl (1-((5-(2-chloro-4-(propylamino)pyrimidin-5-yl)-4-pentyn-1-yl)amino)-1-oxopropan-2-yl)(methyl)carbamate (L1, 910 mg) in 1,4-dioxane (10 mL), a 4.0 mol/L solution of hydrochloric acid in dioxane (7 mL) was added at room temperature, and the mixture was stirred at the same temperature for 1 hour. The solvent was evaporated under reduced pressure to obtain (S)—N-(5-(2-chloro-4-(propylamino)pyrimidin-5-yl)-4-pentyn-1-yl)-2-(methylamino)propanamide (L3) hydrochloride.

후처리

  1. customThe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-8f57190b31c14a3cbc8c7e0b92977523
출처 데이터셋
uspto-grants-2015_09
특허 번호
US09145415B2

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