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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1106112생성일: 2026년 10월 27일

Chlorotrimethylsilane → HCID 178474807, 화합물

https://huagongshe.com/reaction/1106112

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물4-MethylmorpholineHCID 7972—
반응물TriethylamineHCID 8471—
반응물Isobutyl chloroformateHCID 62365—
반응물N-Acetyl-beta-alanineHCID 76406—
반응물HCID 178507442HCID 178507442—
용매AcetonitrileHCID 6342—
용매DichloromethaneHCID 6344—
생성물HCID 178474807HCID 17847480796.3%

반응 조건

온도-10 °C

반응 단계

A solution of 4.6 g (35 mmol) of N-acetyl-beta-alanine, 100 ml acetonitrile, and 3.9 ml (35 mmol) of N-methylmorpholine is stirred at -15° C. and 5.0 ml (38.5 mmol) of isobutyl chloroformate is added. After 30 minutes at -15° C. a solution prepared from 4.05 g (17.5 mmol) of 2-(4-aminophenyl)-4-hydroxy-5-pyrimidine carboxylic acid, 7.35 ml (52.5 mmol) of triethylamine, and 7.96 ml (62.7 mmol) of trimethylsilyl chloride in 100 ml of dichloromethane is added and the mixture stirred at -10° C. for 1 hour and at room temperature overnight. The mixture is evaporated to near dryness in vacuo and treated with 200 ml of water. The product is precipitated by acidifying to pH 2.0 and is filtered, washed with water, isopropanol, ether, and dried to give 5.8 g of 2-[4-(N-acetyl-beta-alanylamino)phenyl]-4-hydroxy-5-pyrimidine carboxylic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04311699
출처 데이터셋uspto-grants-1982_01
ORD IDord-2899a12b1d5040b5941ba4b0bcb1bad2
출처 메모uspto-grants-1982_01