돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 389670생성일: 2026년 10월 26일

Hydrochloric Acid → (S)-methyl 2-((tert-butoxycarbonyl)amino)-3-(5-chlorothiophene-2-carboxamido)propanoate

https://huagongshe.com/reaction/389670

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물DiisopropylcarbodiimideHCID 12734—
반응물N-HydroxysuccinimideHCID 80170—
반응물DiisopropylethylamineHCID 81531—
반응물5-Chloro-2-thiophenecarboxylic acidHCID 95048—
반응물TrimethylsilyldiazomethaneHCID 167693—
반응물Boc-Dap-OHHCID 2755946—
용매DichloromethaneHCID 6344—
생성물(S)-methyl 2-((tert-butoxycarbonyl)amino)-3-(5-chlorothiophene-2-carboxamido)propanoateHCID 6715529091.1%

반응 단계

Commercially available (S)-3-amino-2-tert-butoxycarbonylamino-propionic acid (BOC-Dap-OH) (18.09 g, 88.56 mmol) was suspended in 100 ml DCM with N-hydroxy-succinimide (16.99 g, 147.61 mmol) and N,N′-diisopropylcarbodiimide (11.43 ml, 73.8 mmol), then 5-Chloro-thiophene-2-carboxylic acid (12 g, 73.8 mmol) and DIPEA (25.51 ml, 147.61 mmol) in 60 ml DCM were slowly added. The mixture was stirred at RT for 2 h, then cooled to 0° C. and TMS-diazomethane was slowly added. The reaction was stirred for 2 h at RT, HCl solution (0.5 M) was added and the organic layer was separated, washed with H2O, dried with Na2SO4, filtered and evaporated to dryness. The resulting solid was triturated 16 h with diisopropyl ether, filtered and washed with diisopropyl ether and dried under vacuum at 60° C. 24.4 g of crude product were obtained and used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08378092B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-c93bffd3f83441cabd5fc5ba89627ea6
출처 메모uspto-grants-2013_02