Sodium Hydroxide → HCID 178442041、化合物

HRID 540394ノート

反応式

HRID 540394 の反応式
CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F.Cl.[CH2:24]([C:31]([OH:33])=O)[CH2:25][C:26]1[N:30]=[CH:29][NH:28][CH:27]=1.[NH2:34][C@H:35]([CH2:54][C:55]1[CH:60]=[CH:59][C:58]([O:61][CH3:62])=[CH:57][CH:56]=1)[C:36]([N:38]1[CH2:41][C:40]([CH2:49][CH2:50][CH2:51][CH2:52][CH3:53])([C:42]2[CH:47]=[CH:46][C:45]([F:48])=[CH:44][CH:43]=2)[CH2:39]1)=[O:37].[OH-].[Na+]>CN(C)C=O.C(N(CC)CC)C>[F:48][C:45]1[CH:46]=[CH:47][C:42]([C:40]2([CH2:49][CH2:50][CH2:51][CH2:52][CH3:53])[CH2:39][N:38]([C:36](=[O:37])[C@H:35]([NH:34][C:31](=[O:33])[CH2:24][CH2:25][C:26]3[N:30]=[CH:29][NH:28][CH:27]=3)[CH2:54][C:55]3[CH:60]=[CH:59][C:58]([O:61][CH3:62])=[CH:57][CH:56]=3)[CH2:41]2)=[CH:43][CH:44]=1

参加物

7

反応物 4

HCID 14798Sodium HydroxideHCID 2733207O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 66988297(R)-2-Amino-3-(4-methoxyphenyl)-1-(3-pentyl-3-(4-fluorophenyl)azetidin-1-yl)-propan-1-oneHCID 178479756HCID 178479756、化合物

生成物 1

HCID 178442041HCID 178442041、化合物収率 61%

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒2 回HCID 8471Triethylamine溶媒

実験手順

600 mg (1.86 mmol) of TBTU and 0.45 ml of triethylamine are added to a solution containing 330 mg (1.86 mmol) of desamino-histidine hydrochloride in 5 ml of dimethylformamide. After stirring for 15 minutes, 590 mg (1.55 mmol) of (R)-2-amino-3-(4-methoxyphenyl)-1-(3-pentyl-3-(4-fluorophenyl)azetidin-1-yl)-propan-1-one dissolved in 5 ml of dimethylformamide are added. The reaction medium is stirred at ambient temperature for 3 days. The reaction is stopped by adding a 1N solution of sodium hydroxide and then extracted with a 1/1 heptane/ethyl acetate mixture. The organic phases are combined and dried over sodium sulphate. After filtration, the solvents are evaporated off and the residue is then purified by silica gel chromatography (eluent 85/15 dichloromethane/methanol). 490 mg of N-[(R)-2-[3-(4-fluorophenyl)-3-pentylazetidin-1-yl]-1-(4-methoxybenzyl)-2-oxoethyl]-3-(1H-imidazol-4-yl)-propionamide are obtained in the form of a white powder with a yield of 61%.

後処理

  1. additionare added
  2. stirringThe reaction medium is stirred at ambient temperature for 3 days
  3. extractionextracted with a 1/1 heptane/ethyl acetate mixture
  4. dry with materialdried over sodium sulphate
  5. filtrationAfter filtration
  6. customthe solvents are evaporated off
  7. customthe residue is then purified by silica gel chromatography (eluent 85/15 dichloromethane/methanol)

出典と根拠

ORDレコード
ord-a7471c4989fc46b7873e58c88fab5d35
出典データセット
uspto-grants-2014_10
特許番号
US08871187B2

反応ノート

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