Triethylamine → HCID 178431944, compound

HRID 1764384Notes

Reaction equation

HRID 1764384 reaction equation
[NH2:1][CH:2]1[C:15](=[O:16])[N:4]2[CH:5]([C:10]3[NH:14][N:13]=[N:12][N:11]=3)[C:6]([CH3:9])([CH3:8])[S:7][C@H:3]12.C(N(CC)CC)C.Cl.[Cl:25][C:26]1[CH:31]=[CH:30][C:29]([CH2:32][C:33]([NH:35][C:36](=[O:42])[NH:37][CH2:38][C:39](Cl)=[O:40])=[NH:34])=[CH:28][CH:27]=1>CN(C)C=O>[Cl:25][C:26]1[CH:27]=[CH:28][C:29]([CH2:32][C:33]([NH:35][C:36](=[O:42])[NH:37][CH2:38][C:39]([NH:1][CH:2]2[C:15](=[O:16])[N:4]3[CH:5]([C:10]4[NH:11][N:12]=[N:13][N:14]=4)[C:6]([CH3:8])([CH3:9])[S:7][C@H:3]23)=[O:40])=[NH:34])=[CH:30][CH:31]=1

Participants

5

Procedure

To a stirred solution of 480 mg. of 6-amino-2,2-dimethyl-3-(5-tetrazolyl)penam and 404 mg. of triethylamine, in 6 ml. of N,N-dimethylformamide, is added 650 mg. of 2-(3-[2-(p-chlorophenyl)acetimidoyl]ureido)acetyl chloride hydrochloride. Stirring is continued for 1 hour, and then the reaction mixture is filtered. The filtrate is added to 300 ml. of ether, and the solid which precipitates is filtered off. The solid is washed thoroughly with methylene chloride, and dried, giving 585 mg. of the title compound, m.p. 150°-162° C. IR spectrum (Nujol mull): 1780 cm-1 (β-lactam). NMR spectrum (DMSO-d6): 8.90 ppm (d, 1H), 8.00-7.20 ppm (m, 8H), 5.80-5.20 ppm (m, 3H), 4.10-3.60 ppm (m, 4H), 1.65 ppm (s, 3H), 1.10 ppm (s, 3H).

Workup

  1. filtrationthe reaction mixture is filtered
  2. additionThe filtrate is added to 300 ml
  3. customof ether, and the solid which precipitates
  4. filtrationis filtered off
  5. washThe solid is washed thoroughly with methylene chloride
  6. customdried
  7. customgiving 585 mg

Sources & evidence

ORD record
ord-d58bff177cc449519c9641f2f3c0f28c
Source dataset
uspto-grants-1978_09
Patent number
US04115385

Reaction notes

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