4-Toluenesulfonyl chloride → cis 4-Thiocyanatomethyl-3-[2-(2-tritylamino-4-thiazolyl)-2-methoxyimino-acetamido]-2-oxo-azetidine

HRID 1199589ノート

反応式

HRID 1199589 の反応式
S(Cl)(C1C=CC(C)=CC=1)(=O)=O.[C:12]([NH:31][C:32]1[S:33][CH:34]=[C:35]([C:37](=[N:41][O:42][CH3:43])[C:38]([OH:40])=O)[N:36]=1)([C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)([C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.Cl.[S:45]([CH2:48][C@H:49]1[NH:52][C:51](=[O:53])[C@H:50]1[NH2:54])[C:46]#[N:47]>C(Cl)Cl.C(N(CC)CC)C>[S:45]([CH2:48][C@H:49]1[NH:52][C:51](=[O:53])[C@H:50]1[NH:54][C:38](=[O:40])[C:37]([C:35]1[N:36]=[C:32]([NH:31][C:12]([C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)([C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=2)[C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=2)[S:33][CH:34]=1)=[N:41][O:42][CH3:43])[C:46]#[N:47]

参加物

6

反応物 3

HCID 73974-Toluenesulfonyl chlorideHCID 2724510(Z)-2-(2-Tritylaminothiazol-4-yl)-2-methoxyiminoacetic acidHCID 86743760cis 4-Thiocyanatomethyl-3-amino-2-oxo-azetidine hydrochloride

生成物 1

HCID 86743762cis 4-Thiocyanatomethyl-3-[2-(2-tritylamino-4-thiazolyl)-2-methoxyimino-acetamido]-2-oxo-azetidine

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒2 回HCID 8471Triethylamine溶媒2 回

実験手順

1 ml of triethylamine and then 1.38 g of tosyl chloride were added to a suspension of 3.19 g of the syn isomer of 2-(2-tritylamino-4-thiazolyl)-2-methoxyimino-acetic acid in 50 ml of methylene chloride and the mixture was stirred at room temperature for 40 minutes. A solution of 1.162 g of the product of Step C in 40 ml of methylene chloride and 2 ml of trietylamine were added to the mixture over 5 minutes and the mixture was stirred for 4 hours, was washed with water, then with water containing 4 ml of N hydrochloric acid, dried and evaporated to dryness. The residue was dissolved in ethyl acetate and the solution was iced and vacuum filtered. The product was washed with methanol and dried to obtain 0.709 g of racemate of syn isomer of cis 4-thiocyanatomethyl-3-[2-(2-tritylamino-4-thiazolyl)-2-methoxyimino-acetamido]-2-oxo-azetidine. The mother liquors were evaporated to dryness and the residue was chromatographed over silica gel. Elution with a 93-7 chloroform-methanol mixture yielded another 1.069 g of the said product.

後処理

  1. stirringthe mixture was stirred for 4 hours
  2. washwas washed with water
  3. dry with materialwith water containing 4 ml of N hydrochloric acid, dried
  4. customevaporated to dryness
  5. dissolutionThe residue was dissolved in ethyl acetate
  6. filtrationvacuum filtered
  7. washThe product was washed with methanol
  8. customdried

出典と根拠

ORDレコード
ord-015153e4c96f4fb39c208fca3029f56b
出典データセット
uspto-grants-1990_02
特許番号
US04900728

反応ノート

読み込み中…