Lithium hydroxide, monohydrate → {6-Chloro-3-methyl-4-[4-(piperidine-1-sulfonyl)-phenyl]-naphthalen-2-yl}-acetic acid

HRID 1468415노트

반응식

HRID 1468415 반응식
O.[OH-].[Li+].C[O:5][C:6](=[O:35])[CH2:7][C:8]1[C:17]([CH3:18])=[C:16]([C:19]2[CH:24]=[CH:23][C:22]([S:25]([N:28]3[CH2:33][CH2:32][CH2:31][CH2:30][CH2:29]3)(=[O:27])=[O:26])=[CH:21][CH:20]=2)[C:15]2[C:10](=[CH:11][CH:12]=[C:13]([Cl:34])[CH:14]=2)[CH:9]=1.C1COCC1.O>CCCCCC>[Cl:34][C:13]1[CH:14]=[C:15]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8]([CH2:7][C:6]([OH:35])=[O:5])[C:17]([CH3:18])=[C:16]2[C:19]1[CH:20]=[CH:21][C:22]([S:25]([N:28]2[CH2:33][CH2:32][CH2:31][CH2:30][CH2:29]2)(=[O:26])=[O:27])=[CH:23][CH:24]=1

참가 물질

5

반응물 3

HCID 168937Lithium hydroxide, monohydrateHCID 21881883Oxolane--water (1/1)HCID 86695007{6-Chloro-3-methyl-4-[4-(piperidine-1-sulfonyl)-phenyl]-naphthalen-2-yl}-acetic acid methyl ester

생성물 1

HCID 71711380{6-Chloro-3-methyl-4-[4-(piperidine-1-sulfonyl)-phenyl]-naphthalen-2-yl}-acetic acid수율 101.1%

시약·촉매·용매 1

HCID 8058Hexane용매

실험 절차

Lithium hydroxide monohydrate (0.046 g, 1.1 mmol) was added to a stirred solution of {6-chloro-3-methyl-4-[4-(piperidine-1-sulfonyl)-phenyl]-naphthalen-2-yl}-acetic acid methyl ester (0.130 g, 0.27 mmol) in a 3:1 mixture of THF—H2O mixture (15 mL). The reaction mixture was stirred for 16 hours at room temperature. The reaction mixture was concentrated to remove THF, and the crude material was diluted with water, acidified [pH˜2] with a 6 N aqueous solution of hydrochloric acid. The mixture was extracted twice with ethyl acetate. The collected organic layers were washed with water and brine, dried over anhydrous Na2SO4, and concentrated under reduced pressure to give the crude product. Trituration with hexane afforded {6-chloro-3-methyl-4-[4-(piperidine-1-sulfonyl)-phenyl]-naphthalen-2-yl}-acetic acid (0.125 g, 99%) as a solid. 1H NMR (DMSO-d6) δ: 12.51 (br. s, 1H), 7.98 (d, J=8.8 Hz, 1H), 7.88-7.95 (m, 3H), 7.53 (d, J=8.3 Hz, 2H), 7.50 (dd, J=8.8, 1.5 Hz, 1H), 7.01 (s, 1H), 3.87 (s, 2H), 3.02 (t, J=4.9 Hz, 4H), 2.08 (s, 3H), 1.59 (br. s, 4H), 1.33-1.49 (m, 2H). MS calcd. for C24H25ClNO4S [(M+H)+] 458, obsd. 458.4.

후처리

  1. concentrationThe reaction mixture was concentrated
  2. customto remove THF
  3. additionthe crude material was diluted with water
  4. extractionThe mixture was extracted twice with ethyl acetate
  5. washThe collected organic layers were washed with water and brine
  6. dry with materialdried over anhydrous Na2SO4
  7. concentrationconcentrated under reduced pressure
  8. customto give the crude product

출처 및 근거

ORD 기록
ord-c4d33ec64ecf42bd8e0e0e471e1e2821
출처 데이터셋
uspto-grants-2015_04
특허 번호
US09000044B2

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