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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426994Generated: October 30, 2026

Triethylamine → HCID 178521132, compound

https://huagongshe.com/reaction/426994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
ReactantBistrimethylsilylacetamidHCID 11708267—
ReactantHCID 178524938HCID 178524938—
SolventDichloromethaneHCID 6344—
ProductHCID 178521132HCID 178521132—

Reaction Steps

In a similar manner to that of Example 1-4), 3-mercapto-5-hydroxy-1,2,4-triazine-6-carbonyl chloride, which was prepared from 3-mercapto-5-hydroxy-1,2,4-triazine-6-carboxylic acid (1.73 g), triethylamine (1.0 g), dimethyllformamide (30 ml) and thionyl chloride (1.19 g), was treated with a mixture of 7-(D-2-phenylglycinamido)-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid (4.0 g) and bis(trimethylsilyl) acetamide (6.4 g) in methylene chloride (40 ml). Thus obtained reaction mixture was worked up in a similar manner to that of Example 1--1) to give power (870 mg) of 7-[D-2-(3-mercapto-5-hydroxy-1,2,4-triazine-6-carboxamido)-2-phenylacetamido]-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid, mp 175° to 179° C. (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04172198
Source datasetuspto-grants-1979_10
ORD IDord-0eec236ff0364cecbf03bf29383700be
Source noteuspto-grants-1979_10