1,2-Dichloroethane → (5S,11R)-22-chloro-11-cyclohexyl-18-oxa-3,9,12,15-tetrazatricyclo[17.4.0.05,9]tricosa-1(19),20,22-triene-4,10,13,16-tetrone

HRID 6687

反応式

HRID 6687 の反応式
C([O:5][C:6]([NH:8][C@H:9]([CH:33]1[CH2:38][CH2:37][CH2:36][CH2:35][CH2:34]1)[C:10]([N:12]1[CH2:16][CH2:15][CH2:14][C@H:13]1[C:17]([NH:19][CH2:20][C:21]1[CH:31]=[C:30]([Cl:32])[CH:29]=[CH:28][C:22]=1[O:23][CH2:24][C:25]([OH:27])=O)=[O:18])=[O:11])=O)(C)(C)C.Cl.C(OC(=O)[CH2:46][NH2:47])(C)(C)C.C(N(CC)CC)C.C1C=NC2N(O)N=NC=2C=1.C(Cl)CCl>CN(C=O)C.CCOC(C)=O>[Cl:32][C:30]1[CH:29]=[CH:28][C:22]2[O:23][CH2:24][C:25](=[O:27])[NH:47][CH2:46][C:6](=[O:5])[NH:8][C@H:9]([CH:33]3[CH2:38][CH2:37][CH2:36][CH2:35][CH2:34]3)[C:10](=[O:11])[N:12]3[CH2:16][CH2:15][CH2:14][C@H:13]3[C:17](=[O:18])[NH:19][CH2:20][C:21]=2[CH:31]=1

参加物

8

反応条件

温度
0 °C

実験手順

To a solution of 0.049 g (0.09 mmol) [2-({[((2S)-1-{(2R)-2-[(tert-butoxycarbonyl) amino]-2-cyclohexylethanoyl} pyrrolidin-2-yl)carbonyl]amino} methyl)-4-chlorophenoxy]acetic acid (J. Med. Chem 1998, 41, 3210) in 3 mL DMF was added 0.018 g (0.1 mmol) glycine tertbutyl ester hydrochloride, 0.015 mL (0.1 mmol) triethylamine, 0.014 g (0.1 mmol) HOAt and 0.029 g (0.15 mmol) EDC. After 3 hours the reaction mixture was diluted with 100 mL EtOAc, washed with 50 mL each of 10% aqueous KHSO4, dilute brine, and brine, then dried over Na2SO4, filtered, and concentrated. The residue was dissolved in 3 mL CH2Cl2 and cooled to 0° C. whereupon 1.5 mL trifluoroacetic acid was added and the mixture stirred 30 minutes at 0° C. then warmed to room temperature for 2 hours. To this was added 50 mL toluene and the mixture concentrated, redissolved in CH2Cl2 and toluene and concentrated. The residue was dissolved in 50 mL DMF and to this was added 0.03 mL (0.2 mmol) triethylamine, 0.015 g (0.1 mmol) HOAt and 0.030 g (0.15 mmol) EDC. After 64 hours the reaction mixture was concentrated and the residue diluted with 50 mL EtOAc, washed with 20 mL each of 10% aqueous KHSO4, dilute brine, and brine, then dried over Na2SO4, filtered, and concentrated. Purification by flash chromatography (1.5×12 cm silica gel, linear gradient 1–9% MeOH/CH2Cl2 afforded (6R,20aS)-16-chloro-6-cyclohexyl-2,3,6,7,9,10,18,19-octahydro-1H-pyrrolo[1,2-j][1,4,7,10,13] benzoxatetraazacyclohexadecine-5,8,11,20 (12H,20aH)-tetrone as a white flaky solid. 1H NMR (CD3OD, 400 MHz): δ 7.32 (d, J=2.65 Hz, 1H), 7.24 (dd, J=2.65 and 8.8 Hz, 1H), 7.01 (d, J=8.8 Hz, 1H), 4.75 (d, J=14.0 Hz, 1H), 4.69 (d, J=14.3 Hz, 1H), 4.60 (d, J=14.3 Hz, 1H); 4.45 (dd, J=3.2 and 8.5 Hz, 1H), 4.3 (d, J=9.97 Hz, 1H), 4.15 (d, J=15.6 Hz, 1H), 4.13 (d, J=14.0 Hz, 1H), 3.97 (m, 1H), 3.73 (d, J=15.6 Hz, 1H), 3.61 (m, 1H), 2.16 (m, 1H), 2.08 (m, 1H), 2.0–1.88 (m, 3H), 1.8–1.6 (m, 5H), 1.58 (m, 1H), 1.28 (m, 2H), 1.04 (m, 1H); exact mass calculated for C24H31C1N4O5: 491.2056 found 491.2067. Analytical HPLC (Zorbax SB-C18 4.6×75 mm, 5% to 95% CH3CN in 0.1% aqueous H3PO4):>99% at 215 nm.

後処理

  1. washwashed with 50 mL each of 10% aqueous KHSO4, dilute brine, and brine
  2. dry with materialdried over Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated
  5. dissolutionThe residue was dissolved in 3 mL CH2Cl2
  6. additionwas added
  7. temperaturethen warmed to room temperature for 2 hours
  8. additionTo this was added 50 mL toluene
  9. concentrationthe mixture concentrated
  10. dissolutionredissolved in CH2Cl2
  11. concentrationtoluene and concentrated
  12. dissolutionThe residue was dissolved in 50 mL DMF
  13. concentrationAfter 64 hours the reaction mixture was concentrated
  14. additionthe residue diluted with 50 mL EtOAc
  15. washwashed with 20 mL each of 10% aqueous KHSO4, dilute brine, and brine
  16. dry with materialdried over Na2SO4
  17. filtrationfiltered
  18. concentrationconcentrated
  19. customPurification by flash chromatography (1.5×12 cm silica gel, linear gradient 1–9% MeOH/CH2Cl2

出典と根拠

ORDレコード
ord-a9969a0f2f7a4f47a1fe7d91077a1b28
出典データセット
uspto-grants-2006_08
特許番号
US07084134B2

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