Hydrochloric Acid → (S)-2-{[(1R,2R,4S)-2-{(S)-1-[((S)-Cyclohexyl-methylcarbamoyl-methyl)-carbamoyl]-2,2-dimethyl-propylcarbamoyl}-4-(7-methoxy-2-phenyl-quinolin-4-yloxy)-cyclopentanecarbonyl]-amino}-pentanoic acid tert-butyl ester

HRID 2242430ノート

反応式

HRID 2242430 の反応式
CO[C:3]([C@@H:5]1[CH2:9][C@H:8]([O:10][C:11]2[C:20]3[C:15](=[CH:16][C:17]([O:21][CH3:22])=[CH:18][CH:19]=3)[N:14]=[C:13]([C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)[CH:12]=2)[CH2:7][C@H:6]1[C:29](=[O:42])[NH:30][C@H:31]([C:35]([O:37][C:38]([CH3:41])([CH3:40])[CH3:39])=[O:36])[CH2:32][CH2:33][CH3:34])=[O:4].[Li+].[OH-].Cl.C(OC(=O)[NH:52][C@H:53]([C:58](=[O:71])[NH:59][C@@H:60]([CH:65]1[CH2:70][CH2:69][CH2:68][CH2:67][CH2:66]1)[C:61](=[O:64])[NH:62][CH3:63])[C:54]([CH3:57])([CH3:56])[CH3:55])(C)(C)C.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C(OC([C@@H]1C[C@@H](O)C[C@H]1C(=O)N[C@]1(C(OCC)=O)C[C@H]1C=C)=O)(C)(C)C>O1CCOCC1.O.CN(C=O)C>[C:38]([O:37][C:35](=[O:36])[C@@H:31]([NH:30][C:29]([C@@H:6]1[CH2:7][C@@H:8]([O:10][C:11]2[C:20]3[C:15](=[CH:16][C:17]([O:21][CH3:22])=[CH:18][CH:19]=3)[N:14]=[C:13]([C:23]3[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=3)[CH:12]=2)[CH2:9][C@H:5]1[C:3](=[O:4])[NH:52][C@H:53]([C:58](=[O:71])[NH:59][C@@H:60]([CH:65]1[CH2:66][CH2:67][CH2:68][CH2:69][CH2:70]1)[C:61](=[O:64])[NH:62][CH3:63])[C:54]([CH3:56])([CH3:57])[CH3:55])=[O:42])[CH2:32][CH2:33][CH3:34])([CH3:40])([CH3:41])[CH3:39]

参加物

9

反応物 6

HCID 313Hydrochloric AcidHCID 3939Lithium HydroxideHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 57892933{(S)-1-[((S)-Cyclohexyl-methylcarbamoyl-methyl)-carbamoyl]-2,2-dimethyl-propyl}-carbamic acid tert-butyl esterHCID 59165438(1R,2R,4S)-2-((1R,2S)-1-Ethoxycarbonyl-2-vinyl-cyclopropylcarbamoyl) 4-hydroxy-cyclopentanecarboxylic acid tert-butyl esterHCID 59204183(1R,2R,4R)-2-((S)-1-tert-Butoxycarbonyl-butylcarbamoyl)-4-(7-methoxy-2-phenyl-quinolin-4-yloxy)-cyclopentanecarboxylic acid methyl ester

生成物 1

HCID 59204189(S)-2-{[(1R,2R,4S)-2-{(S)-1-[((S)-Cyclohexyl-methylcarbamoyl-methyl)-carbamoyl]-2,2-dimethyl-propylcarbamoyl}-4-(7-methoxy-2-phenyl-quinolin-4-yloxy)-cyclopentanecarbonyl]-amino}-pentanoic acid tert-butyl ester収率 81%

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 218864351,4-Dioxane--water (1/1)溶媒

反応条件

温度
0 °C

実験手順

Compound 43 (38 mg, 0.066 mmol) was dissolved in dioxane/water 1:1 (4 mL) and the solution was cooled to 0° C. and 1 M LiOH (132 ul, 0.132 mmol) was added. The temperature was raised to room temperature and the solution was stirred for 2 hours after which it was neutralized by addition of 1M HCl and evaporated and coevaporated with toluene. The residue and deprotected amine 38 (1.1 eq) was dissolved in DMF and coupled using the standard HATU coupling conditions as in the synthesis of compound 34. The crude product was extracted with EtOAc, washed with brine, dried, filtered and concentrated. Purification with HPLC (MeOH/water 9:1+0.2% TEA) provided compound 44 (44 mg, 81%) as a colorless solid.

後処理

  1. temperatureThe temperature was raised to room temperature
  2. customevaporated
  3. extractionThe crude product was extracted with EtOAc
  4. washwashed with brine
  5. customdried
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customPurification with HPLC (MeOH/water 9:1+0.2% TEA)

出典と根拠

ORDレコード
ord-13e3031341644732949a319c87fbb654
出典データセット
uspto-grants-2010_03
特許番号
US07671032B2

反応ノート

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