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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764377Generated: November 1, 2026

Triethylamine → HCID 178464571, compound

https://huagongshe.com/reaction/1764377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN,N'-DiethylthioureaHCID 2735009—
ReactantHCID 178431923HCID 178431923—
SolventDichloromethaneHCID 6344—
ProductHCID 178464571HCID 178464571—

Reaction Steps

To a stirred solution of 1.40 g (0.039 mole) of 6-(2-bromoacetamido)-2,2-dimethyl-3-(5-tetrazolyl)penam in 25 ml of methylene chloride is added 0.54 ml (0.039 mole) of triethylamine, followed by 0.52 g (0.039 mole) of N,N'-diethylthiourea. Stirring is continued for a further 45 minutes, and then the solvent is decanted from the oil which has separated. The oil is triturated with ether, giving a white solid, which is filtered off. The yield is 1.28 g (76% of theory) of 6-(2-[N,N'-diethylamidinothio]acetamido)-2,2-dimethyl-3-(5-tetrazolyl)penam. The infrared spectrum (KBr disc) of the product shows absorption bands at 1780 cm-1 (β-lactam) and 1670 cm-1 (amide I). The NMR spectrum (DMSO-d6) shows absorption bands at 5.65 ppm (multiplet, C-5 and C-6 hydrogens), 5.15 ppm (singlet, C-3 hydrogen), 4.10 ppm (singlet, methylene hydrogens), 3.45 ppm (quartet, ethyl hydrogens), 1.60 ppm (singlet, C-2 methyl hydrogens), 1.10 ppm (triplet, ethyl hydrogens) and 1.00 ppm (singlet, C-2 methyl hydrogens).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04115385
Source datasetuspto-grants-1978_09
ORD IDord-f705d92e47144ef2bd8c2b8f37110039
Source noteuspto-grants-1978_09