Hydrochloric Acid → HCID 66894003, 화합물

HRID 1921231노트

반응식

HRID 1921231 반응식
C(OC([N:8]1[CH2:17][CH2:16][C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH:9]1[C:18]([OH:20])=[O:19])=O)(C)(C)C.[OH:21][NH:22][C:23](=[NH:25])[CH3:24].[ClH:26].[CH3:27]N(C)CCCN=C=NCC.ON1C2C=CC=CC=2N=N1.Cl.O1CCOCC1>>[ClH:26].[CH3:24][C:23]1[N:25]=[C:27]([C:9]2([C:18]([OH:20])=[O:19])[C:10]3[C:15](=[CH:14][CH:13]=[CH:12][CH:11]=3)[CH2:16][CH2:17][NH:8]2)[O:21][N:22]=1

참가 물질

7

실험 절차

A solution of 2-(tert-butyoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid (2.00 g, 7.21 mmol), N-hydroxyacetamidine (1.39 g, 18.8 mmol), [3-(dimethylamino)propyl]ethyl carbodiimide hydrochloride (3.04 g, 15.9 mmol), and 1-hydroxybenzotriazole (1.55 g, 1.01 mmol) was heated to 100° C. for 18 hours, then cooled to rt and concentrated in vacuo. The resultant residue was redissolved in ethyl acetate and washed with saturated aqueous sodium bicarbonate and brine, dried over sodium sulfate, filtered, concentrated in vacuo, and subjected to silica gel chromatography from 0 to 20% ethyl actate in hexanes. To a solution of the resultant compound (0.600 g, 1.90 mmol) was added 4 N HCl in dioxane (1.42 mL, 4.26 mmol). After 2 hours, the reaction was concentrated in vacuo to provide the title compound as a beige solid that gave a proton NMR spectrum consistent with theory and a mass ion (ES+) of 216.2. This crude intermediate was used to prepare Example 21, by the procedure described for Example 1.

후처리

  1. concentrationconcentrated in vacuo
  2. dissolutionThe resultant residue was redissolved in ethyl acetate
  3. washwashed with saturated aqueous sodium bicarbonate and brine
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. concentrationthe reaction was concentrated in vacuo

출처 및 근거

ORD 기록
ord-377689efef6a4d06bdc6ab4224c10de7
출처 데이터셋
uspto-grants-2012_05
특허 번호
US08173672B2

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