Trifluoroacetic acid → Trifluoroacetic acid
반응식
C(OC([NH:8][C@H:9]1[CH2:14][CH2:13][CH2:12][CH2:11][C@H:10]1[NH:15][C:16]1[N:21]=[C:20]([C:22]2[S:26][C:25]([NH:27]C(=O)OC(C)(C)C)=[N:24][CH:23]=2)[C:19]2[C:35](=[O:49])[N:36](CC3C=CC(OC)=CC=3OC)[CH2:37][C:18]=2[C:17]=1[F:50])=O)(C)(C)C.[C:51]([OH:57])([C:53]([F:56])([F:55])[F:54])=[O:52]>>[NH2:8][C@H:9]1[CH2:14][CH2:13][CH2:12][CH2:11][C@H:10]1[NH:15][C:16]1[N:21]=[C:20]([C:22]2[S:26][C:25]([NH2:27])=[N:24][CH:23]=2)[C:19]2[C:35](=[O:49])[NH:36][CH2:37][C:18]=2[C:17]=1[F:50].[C:51]([OH:57])([C:53]([F:56])([F:55])[F:54])=[O:52]참가 물질
반응물 2
생성물 2
실험 절차
A solution of tert-butyl (5-(6-(((1R,2S)-2-((tert-butoxycarbonyl)amino)cyclo-hexyl)amino)-2-(2,4-dimethoxybenzyl)-7-fluoro-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-4-yl)-1,3-thiazol-2-yl)carbamate (41.5 mg, 0.058 mmol) in TFA (5 mL) was heated to 65° C. for 3 h. After removal of the solvent, the resulting crude material was reconstituted in MeOH/DMF (6.0 mL) and purified via preparative HPLC eluting with water (0.05% TFA) and ACN (10-20% gradient, 0.035% TFA). The collected fractions were stripped to dryness via rotary evaporation to yield the title compound as a TFA salt (6.7 mg, 32%). 1H NMR (400 MHz, DMSO-d6) δ ppm 1.12-2.11 (m, 9H), 3.73 (br s, 2H), 4.19 (d, J=3.79 Hz, 1H), 4.41 (d, J=3.03 Hz, 2H), 6.95 (d, J=3.03 Hz, 1H), 7.77 (br s, 2H), 8.44 (s, 1H), 8.93 (s, 1H). [M+H] calc'd for C16H19FN6OS, 363. found, 363.
후처리
- customAfter removal of the solvent
- custompurified via preparative HPLC
- washeluting with water (0.05% TFA) and ACN (10-20% gradient, 0.035% TFA)
- customThe collected fractions were stripped to dryness via rotary evaporation
출처 및 근거
- ORD 기록
- ord-848403720dc8437d84cfd773181b5be6
- 출처 데이터셋
- uspto-grants-2015_11
- 특허 번호
- US09181255B2
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