Triphenylphosphine → HCID 118307766、化合物

HRID 718455ノート

反応式

HRID 718455 の反応式
[C:1]([O:5][C@@H:6]([C:12]1[C:13]([CH3:34])=[N:14][C:15]([CH3:33])=[C:16]([C:26]2[CH:31]=[CH:30][C:29](O)=[CH:28][CH:27]=2)[C:17]=1[N:18]1[CH2:23][CH2:22][C:21]([CH3:25])([CH3:24])[CH2:20][CH2:19]1)[C:7]([O:9]CC)=[O:8])([CH3:4])([CH3:3])[CH3:2].[CH3:35][C:36]1[S:40][C:39]([CH2:41][CH2:42][OH:43])=[CH:38][CH:37]=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.CC(OC(/N=N/C(OC(C)C)=O)=O)C.[OH-].[Na+]>C1COCC1.CO>[C:1]([O:5][C@@H:6]([C:12]1[C:13]([CH3:34])=[N:14][C:15]([CH3:33])=[C:16]([C:26]2[CH:27]=[CH:28][C:29]([O:43][CH2:42][CH2:41][C:39]3[S:40][C:36]([CH3:35])=[CH:37][CH:38]=3)=[CH:30][CH:31]=2)[C:17]=1[N:18]1[CH2:19][CH2:20][C:21]([CH3:25])([CH3:24])[CH2:22][CH2:23]1)[C:7]([OH:9])=[O:8])([CH3:4])([CH3:2])[CH3:3]

参加物

8

反応物 5

HCID 11776TriphenylphosphineHCID 14798Sodium HydroxideHCID 5363146Diisopropyl azodicarboxylateHCID 1328928919498-70-5HCID 118314205(S)-ethyl 2-(tert-butoxy)-2-(4-(4,4-dimethylpiperidin-1-yl)-5-(4-hydroxyphenyl)-2,6-dimethylpyridin-3-yl)acetate

生成物 1

HCID 118307766HCID 118307766、化合物収率 21.57%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

To a stirred solution of (S)-ethyl 2-(tert-butoxy)-2-(4-(4,4-dimethylpiperidin-1-yl)-5-(4-hydroxyphenyl)-2,6-dimethylpyridin-3-yl)acetate (50 mg, 0.107 mmol), 2-(5-methylthiophen-2-yl)ethanol (76 mg, 0.533 mmol) and Ph3P (139 mg, 0.533 mmol) in THF (2 mL) was added DIAD (0.104 mL, 0.533 mmol) at rt. After 18 h, mixture was filtered to remove polymer, concentrated and treated with 1N NaOH (0.854 mL, 0.854 mmol) in MeOH (1 mL) at 75° C. for 16 h. Mixture was then cooled and purified by prep-HPLC to afford (S)-2-(tert-butoxy)-2-(4-(4,4-dimethylpiperidin-1-yl)-2,6-dimethyl-5-(4-(2-(5-methylthiophen-2-yl)ethoxy)phenyl)pyridin-3-yl)acetic acid (13 mg, 0.023 mmol, 21.57% yield). 1H NMR (500 MHz, DMSO-d6) δ 7.20 (d, J=8.8 Hz, 1H), 7.10-6.91 (m, 4H), 6.73 (d, J=3.3 Hz, 1H), 6.63 (br. s., 1H), 5.82 (s, 1H), 4.29-4.07 (m, 3H), 3.26 (br. s., 1H), 3.17 (t, J=6.1 Hz, 1H), 2.43 (s, 3H), 2.38 (s, 3H), 2.15 (br. s., 1H), 2.05 (s, 3H), 1.28 (br. s., 2H), 1.17 (d, J=16.5 Hz, 1H), 1.11 (s, 9H), 1.07-0.94 (m, 2H), 0.83 (br. s., 3H), 0.60 (br. s., 3H). LCMS (M+H)=565.3.

後処理

  1. filtrationmixture was filtered
  2. customto remove polymer
  3. concentrationconcentrated
  4. temperatureMixture was then cooled
  5. custompurified by prep-HPLC

出典と根拠

ORDレコード
ord-1442174ba8594f86a52b32e815116820
出典データセット
uspto-grants-2015_11
特許番号
US09193720B2

反応ノート

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