1,2-Dichloroethane → Benzyl 9-(5-{[(2-aminophenyl)amino]carbonyl}pyridin-2-yl)-3,9-diazaspiro[5.5]-undecane-3-carboxylate

HRID 1984791

反応式

HRID 1984791 の反応式
C[O:2][C:3]([C:5]1[CH:6]=[CH:7][C:8]([N:11]2[CH2:28][CH2:27][C:14]3([CH2:19][CH2:18][N:17]([C:20]([O:22]C(C)(C)C)=[O:21])[CH2:16][CH2:15]3)[CH2:13][CH2:12]2)=[N:9][CH:10]=1)=O.CCN(CC)CC.C(Cl)(O[CH2:39][C:40]1[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=1)=O.O[Li].O.C(Cl)CCl.[CH:54]1[CH:55]=[CH:56][C:57]2[N:62](O)N=[N:60][C:58]=2[CH:59]=1.C1(N)C=CC=CC=1N>C(Cl)Cl.C(O)(C(F)(F)F)=O.CO.C1COCC1.O>[NH2:60][C:58]1[CH:59]=[CH:54][CH:55]=[CH:56][C:57]=1[NH:62][C:3]([C:5]1[CH:6]=[CH:7][C:8]([N:11]2[CH2:28][CH2:27][C:14]3([CH2:19][CH2:18][N:17]([C:20]([O:22][CH2:39][C:40]4[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=4)=[O:21])[CH2:16][CH2:15]3)[CH2:13][CH2:12]2)=[N:9][CH:10]=1)=[O:2]

参加物

11

反応物 7

HCID 111,2-DichloroethaneHCID 7243O-PhenylenediamineHCID 8471TriethylamineHCID 10387Benzyl chloroformateHCID 757711-HydroxybenzotriazoleHCID 168937Lithium hydroxide, monohydrateHCID 57717452Tert-butyl 9-[5-(methoxycarbonyl)pyridin-2-yl]-3,9-diazaspiro[5.5]undecane-3-carboxylate

生成物 1

HCID 57717481Benzyl 9-(5-{[(2-aminophenyl)amino]carbonyl}pyridin-2-yl)-3,9-diazaspiro[5.5]-undecane-3-carboxylate

試薬・触媒・溶媒 3

HCID 6344Dichloromethane溶媒HCID 6422Trifluoroacetic acid溶媒HCID 21892291Methanol tetrahydrofuran water溶媒

実験手順

A solution of tert-butyl 9-[5-(methoxycarbonyl)pyridin-2-yl]-3,9-diazaspiro[5.5]undecane-3-carboxylate (100 mg, 0.257 mmol) in 1 mL of CH2Cl2 and 1 mL of TFA was stirred for 1 h and concentrated. The oil was redissolved in 2 mL of CH2Cl2 and treated with NEt3 (0.15 mL, 1.08 mmol) and CbzCl (0.060 mL, 0.42 mmol), then stirred for 8 h. The mixture was partitioned between EtOAc and sat'd NaHCO3, dried (Na2SO4), filtered and concentrated. The residue was stirred in 3 mL of 1:1:1 MeOH/THF/water with LiOH.H2O (30 mg, 0.71 mmol) for 10 h, concentrated to dryness, dissolved in 2 mL of DMF, treated with EDC (150 mg, 0.79 mmol), HOBt (100 mg, 0.74 mmol), and phenylenediamine (100 mg, 0.93 mmol). The mixture was stirred for 18 h, concentrated, and triturated with methanol giving the title compound; MS (ESI+): cal'd [M+1]+ 500.3, obs'd 500.3.

後処理

  1. concentrationconcentrated
  2. dissolutionThe oil was redissolved in 2 mL of CH2Cl2
  3. customThe mixture was partitioned between EtOAc
  4. dry with materialdried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated
  7. concentrationconcentrated to dryness
  8. dissolutiondissolved in 2 mL of DMF
  9. stirringThe mixture was stirred for 18 h
  10. concentrationconcentrated
  11. customtriturated with methanol giving the title compound

出典と根拠

ORDレコード
ord-2ba8ca0ffb484d8687178a91911b37ca
出典データセット
uspto-grants-2009_06
特許番号
US07544695B2

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